The (A) over tilde (2)Sigma(+)-(X) over tilde (2)Pi(i) electronic transition of jet-cooled germanium methylidyne has been recorded in the 730-555 nm region by laser-induced fluorescence techniques. The radical was produced in a pulsed electric discharge using tetramethylgermane as the precursor. The band system consists of perpendicular and vibronically induced parallel bands with upper state frequencies of nu(2)'=638/497 cm(-1) and nu(3)'=990/952 cm(-1) for GeCH/GeCD. The (2)Sigma(+)-(2)Pi(3/2) components of the 0(0)(0) bands of GeCH and GeCD and the 2(0)(1) band of GeCH have been recorded with sufficient resolution to assign the transitions of the Ge-70, Ge-72, Ge-74, and Ge-76 isotopomers. The rotational constants of the various hydrogen and germanium isotopomers were used to derive the following molecular structures: r(0)"(Ge-C)=1.775 79(21) Angstrom, r(0)"(C-H)=1.0673(12) Angstrom, r(0)'(Ge- C)=1.673 66(8) Angstrom, and r(0)'(C-H)=1.0589(5) Angstrom. The ground state germanium-carbon bond length is typical for a Ge=C double bond, but in the excited state it corresponds to a triple bond. This is a consequence of promotion of an electron from a nonbonding sigma orbital to a pi bonding orbital to form the ...sigma(1)pi(4)((2)Sigma(+)) excited state. In this study we provide the first experimental value for the length of the germanium-carbon triple bond.