Canonical Allele Identifier: CA1855118679

Gene: TMC1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.72816190C= , CM000671.2:g.72816190C=	GRCh38
NC_000009.11:g.75431106C= , CM000671.1:g.75431106C=	GRCh37
NC_000009.10:g.74620926C=	NCBI36
NG_008213.1:g.299390C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000297784.10:c.1743C= MANE Select	ENSP00000297784.6:p.Ile581=
ENST00000644967.1:c.1305C=	ENSP00000496159.1:p.Ile435=
ENST00000645053.1:c.1258-10679C=	ENSP00000493838.1:n.1258-10679C=
ENST00000645208.2:c.1743C=	ENSP00000494684.1:p.Ile581=
ENST00000645773.1:c.1617C=	ENSP00000493698.1:p.Ile539=
ENST00000645787.1:n.1886C=
ENST00000646619.1:c.1305C=	ENSP00000493726.1:p.Ile435=
ENST00000651183.1:c.1305C=	ENSP00000498723.1:p.Ile435=
ENST00000297784.9:c.1743C=	ENSP00000297784.5:p.Ile581=
ENST00000340019.4:c.1743C=	ENSP00000341433.3:p.Ile581=
ENST00000469455.1:n.224C=
ENST00000486417.5:n.367C=
NM_138691.2:c.1743C=	NP_619636.2:p.Ile581=
XM_011518213.1:c.2331C=	XP_011516515.1:p.Ile777=
XM_017014256.1:c.1746C=	XP_016869745.1:p.Ile582=
NM_138691.3:c.1743C= MANE Select	NP_619636.2:p.Ile581=