Canonical Allele Identifier: CA1855106312

Gene: TMC1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.72789207G= , CM000671.2:g.72789207G=	GRCh38
NC_000009.11:g.75404123G= , CM000671.1:g.75404123G=	GRCh37
NC_000009.10:g.74593943G=	NCBI36
NG_008213.1:g.272407G=

Transcript Alleles

HGVS	Amino-acid Change
NM_138691.3:c.1114G= MANE Select	NP_619636.2:p.Val372=
ENST00000297784.10:c.1114G= MANE Select	ENSP00000297784.6:p.Val372=
NM_138691.2:c.1114G=	NP_619636.2:p.Val372=
ENST00000297784.9:c.1114G=	ENSP00000297784.5:p.Val372=
ENST00000340019.4:c.1114G=	ENSP00000341433.3:p.Val372=
ENST00000644967.1:c.676G=	ENSP00000496159.1:p.Val226=
ENST00000645053.1:c.676G=	ENSP00000493838.1:p.Val226=
ENST00000645208.2:c.1114G=	ENSP00000494684.1:p.Val372=
ENST00000645773.1:c.988G=	ENSP00000493698.1:p.Val330=
ENST00000645787.1:n.1154G=
ENST00000646619.1:c.676G=	ENSP00000493726.1:p.Val226=
ENST00000650689.1:n.1412G=
ENST00000651183.1:c.676G=	ENSP00000498723.1:p.Val226=
XM_011518213.1:c.1702G=	XP_011516515.1:p.Val568=
XM_017014256.1:c.1117G=	XP_016869745.1:p.Val373=