Canonical Allele Identifier: CA401232769

Gene: TMC6

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.78124671G>C , CM000679.2:g.78124671G>C	GRCh38
NC_000017.10:g.76120752G>C , CM000679.1:g.76120752G>C	GRCh37
NC_000017.9:g.73632347G>C	NCBI36
NG_007879.1:g.12737C>G , LRG_118:g.12737C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_001127198.5:c.744C>G MANE Select	NP_001120670.1:p.Tyr248Ter
ENST00000590602.6:c.744C>G MANE Select	ENSP00000465261.1:p.Tyr248Ter
NM_001127198.1:c.744C>G	NP_001120670.1:p.Tyr248Ter
NM_001127198.2:c.744C>G	NP_001120670.1:p.Tyr248Ter
NM_001321185.1:c.744C>G	NP_001308114.1:p.Tyr248Ter
NM_001374593.1:c.744C>G	NP_001361522.1:p.Tyr248Ter
NM_001374594.1:c.744C>G	NP_001361523.1:p.Tyr248Ter
NM_001374596.1:c.744C>G	NP_001361525.1:p.Tyr248Ter
NM_001375353.1:c.744C>G	NP_001362282.1:p.Tyr248Ter
NM_001375354.1:c.744C>G	NP_001362283.1:p.Tyr248Ter
NM_007267.6:c.744C>G , LRG_118t1:c.744C>G	NP_009198.4:p.Tyr248Ter
NM_007267.7:c.744C>G	NP_009198.4:p.Tyr248Ter
NR_168288.1:n.962C>G
NR_168289.1:n.962C>G
NR_168290.1:n.865C>G
NR_168291.1:n.915C>G
ENST00000306591.11:c.744C>G	ENSP00000306405.6:p.Tyr248Ter
ENST00000322914.7:c.744C>G	ENSP00000313408.2:p.Tyr248Ter
ENST00000392467.7:c.744C>G	ENSP00000376260.2:p.Tyr248Ter
ENST00000586271.1:n.478C>G
ENST00000588087.5:n.937C>G
ENST00000589271.5:c.744C>G	ENSP00000468255.1:p.Tyr248Ter
ENST00000589271.6:c.744C>G	ENSP00000468255.2:p.Tyr248Ter
ENST00000589553.5:c.63C>G	ENSP00000465359.1:p.Tyr21Ter
ENST00000590602.5:c.744C>G	ENSP00000465261.1:p.Tyr248Ter
ENST00000592063.6:c.744C>G	ENSP00000466885.2:p.Tyr248Ter
ENST00000593044.5:n.1324C>G
ENST00000698546.1:c.*566C>G	ENSP00000513789.1:n.*566C>G
ENST00000698547.1:c.*62C>G	ENSP00000513790.1:n.*62C>G
ENST00000698548.1:c.744C>G	ENSP00000513791.1:p.Tyr248Ter
ENST00000698549.1:c.*566C>G	ENSP00000513792.1:n.*566C>G
ENST00000698550.1:c.744C>G	ENSP00000513793.1:p.Tyr248Ter
ENST00000698551.1:c.744C>G	ENSP00000513794.1:p.Tyr248Ter
XM_005256995.1:c.744C>G	XP_005257052.1:p.Tyr248Ter
XM_005256996.1:c.744C>G	XP_005257053.1:p.Tyr248Ter
XM_005256997.1:c.744C>G	XP_005257054.1:p.Tyr248Ter
XM_005256998.1:c.63C>G	XP_005257055.1:p.Tyr21Ter
XM_011524255.1:c.744C>G	XP_011522557.1:p.Tyr248Ter
XM_011524256.1:c.634-16C>G	XP_011522558.1:n.634-16C>G
XM_011524257.1:c.-51-16C>G	XP_011522559.1:n.-51-16C>G
XM_011524257.3:c.-51-16C>G	XP_011522559.1:n.-51-16C>G
XM_011524258.1:c.744C>G	XP_011522560.1:p.Tyr248Ter
XM_017024107.1:c.744C>G	XP_016879596.1:p.Tyr248Ter
XM_017024108.1:c.744C>G	XP_016879597.1:p.Tyr248Ter
XM_024450555.1:c.744C>G	XP_024306323.1:p.Tyr248Ter
XM_024450556.1:c.744C>G	XP_024306324.1:p.Tyr248Ter
XM_024450557.1:c.63C>G	XP_024306325.1:p.Tyr21Ter
XR_001752420.1:n.932C>G
XR_243632.1:n.932C>G