Canonical Allele Identifier: CA1855090113

Gene: TMC1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.72751903G= , CM000671.2:g.72751903G=	GRCh38
NC_000009.11:g.75366819G= , CM000671.1:g.75366819G=	GRCh37
NC_000009.10:g.74556639G=	NCBI36
NG_008213.1:g.235103G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000297784.10:c.589G= MANE Select	ENSP00000297784.6:p.Gly197=
ENST00000644967.1:c.151G=	ENSP00000496159.1:p.Gly51=
ENST00000645053.1:c.151G=	ENSP00000493838.1:p.Gly51=
ENST00000645208.2:c.589G=	ENSP00000494684.1:p.Gly197=
ENST00000645773.1:c.463G=	ENSP00000493698.1:p.Gly155=
ENST00000645787.1:n.629G=
ENST00000646619.1:c.151G=	ENSP00000493726.1:p.Gly51=
ENST00000650689.1:n.887G=
ENST00000651183.1:c.151G=	ENSP00000498723.1:p.Gly51=
ENST00000297784.9:c.589G=	ENSP00000297784.5:p.Gly197=
ENST00000340019.4:c.589G=	ENSP00000341433.3:p.Gly197=
NM_138691.2:c.589G=	NP_619636.2:p.Gly197=
XM_011518213.1:c.1177G=	XP_011516515.1:p.Gly393=
XM_017014256.1:c.592G=	XP_016869745.1:p.Gly198=
NM_138691.3:c.589G= MANE Select	NP_619636.2:p.Gly197=