Canonical Allele Identifier: CA401236644
Community Standard Title: NM_001127198.5(TMC6):c.115C>T (p.Gln39Ter)
Gene: TMC6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.78126590G>A , CM000679.2:g.78126590G>A GRCh38
NC_000017.10:g.76122671G>A , CM000679.1:g.76122671G>A GRCh37
NC_000017.9:g.73634266G>A NCBI36
NG_007879.1:g.10818C>T , LRG_118:g.10818C>T
NG_007881.1:g.813G>A , LRG_119:g.813G>A

Transcript Alleles

HGVS Amino-acid Change
NM_001127198.5:c.115C>T MANE Select NP_001120670.1:p.Gln39Ter
ENST00000590602.6:c.115C>T MANE Select ENSP00000465261.1:p.Gln39Ter
NM_001127198.1:c.115C>T NP_001120670.1:p.Gln39Ter
NM_001127198.2:c.115C>T NP_001120670.1:p.Gln39Ter
NM_001321185.1:c.115C>T NP_001308114.1:p.Gln39Ter
NM_001374593.1:c.115C>T NP_001361522.1:p.Gln39Ter
NM_001374594.1:c.115C>T NP_001361523.1:p.Gln39Ter
NM_001374596.1:c.115C>T NP_001361525.1:p.Gln39Ter
NM_001375353.1:c.115C>T NP_001362282.1:p.Gln39Ter
NM_001375354.1:c.115C>T NP_001362283.1:p.Gln39Ter
NM_007267.6:c.115C>T , LRG_118t1:c.115C>T NP_009198.4:p.Gln39Ter
NM_007267.7:c.115C>T NP_009198.4:p.Gln39Ter
NR_168288.1:n.333C>T
NR_168289.1:n.333C>T
NR_168290.1:n.333C>T
NR_168291.1:n.286C>T
ENST00000306591.11:c.115C>T ENSP00000306405.6:p.Gln39Ter
ENST00000322914.7:c.115C>T ENSP00000313408.2:p.Gln39Ter
ENST00000392467.7:c.115C>T ENSP00000376260.2:p.Gln39Ter
ENST00000586126.1:c.63C>T ENSP00000466159.1:p.Ser21=
ENST00000586697.5:n.203C>T
ENST00000588087.5:n.308C>T
ENST00000588792.5:n.333C>T
ENST00000589271.5:c.115C>T ENSP00000468255.1:p.Gln39Ter
ENST00000589271.6:c.115C>T ENSP00000468255.2:p.Gln39Ter
ENST00000589553.5:c.-470C>T ENSP00000465359.1:n.-470C>T
ENST00000590162.1:n.280C>T
ENST00000590602.5:c.115C>T ENSP00000465261.1:p.Gln39Ter
ENST00000591594.5:n.115C>T
ENST00000592063.5:c.115C>T ENSP00000466885.1:p.Gln39Ter
ENST00000592063.6:c.115C>T ENSP00000466885.2:p.Gln39Ter
ENST00000592594.5:c.115C>T ENSP00000467016.1:p.Gln39Ter
ENST00000593044.5:n.303C>T
ENST00000698546.1:c.66C>T ENSP00000513789.1:p.Ser22=
ENST00000698547.1:c.115C>T ENSP00000513790.1:p.Gln39Ter
ENST00000698548.1:c.115C>T ENSP00000513791.1:p.Gln39Ter
ENST00000698549.1:c.66C>T ENSP00000513792.1:p.Ser22=
ENST00000698550.1:c.115C>T ENSP00000513793.1:p.Gln39Ter
ENST00000698551.1:c.115C>T ENSP00000513794.1:p.Gln39Ter
XM_005256995.1:c.115C>T XP_005257052.1:p.Gln39Ter
XM_005256996.1:c.115C>T XP_005257053.1:p.Gln39Ter
XM_005256997.1:c.115C>T XP_005257054.1:p.Gln39Ter
XM_005256998.1:c.-470C>T XP_005257055.1:n.-470C>T
XM_011524255.1:c.115C>T XP_011522557.1:p.Gln39Ter
XM_011524256.1:c.115C>T XP_011522558.1:p.Gln39Ter
XM_011524258.1:c.115C>T XP_011522560.1:p.Gln39Ter
XM_017024107.1:c.115C>T XP_016879596.1:p.Gln39Ter
XM_017024108.1:c.115C>T XP_016879597.1:p.Gln39Ter
XM_024450555.1:c.115C>T XP_024306323.1:p.Gln39Ter
XM_024450556.1:c.115C>T XP_024306324.1:p.Gln39Ter
XM_024450557.1:c.-470C>T XP_024306325.1:n.-470C>T
XR_001752420.1:n.303C>T
XR_243632.1:n.303C>T