Canonical Allele Identifier: CA1855105949

Gene: TMC1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.72788340A= , CM000671.2:g.72788340A=	GRCh38
NC_000009.11:g.75403256A= , CM000671.1:g.75403256A=	GRCh37
NC_000009.10:g.74593076A=	NCBI36
NG_008213.1:g.271540A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000297784.10:c.886A= MANE Select	ENSP00000297784.6:p.Met296=
ENST00000644967.1:c.448A=	ENSP00000496159.1:p.Met150=
ENST00000645053.1:c.448A=	ENSP00000493838.1:p.Met150=
ENST00000645208.2:c.886A=	ENSP00000494684.1:p.Met296=
ENST00000645773.1:c.760A=	ENSP00000493698.1:p.Met254=
ENST00000645787.1:n.926A=
ENST00000646619.1:c.448A=	ENSP00000493726.1:p.Met150=
ENST00000650689.1:n.1184A=
ENST00000651183.1:c.448A=	ENSP00000498723.1:p.Met150=
ENST00000297784.9:c.886A=	ENSP00000297784.5:p.Met296=
ENST00000340019.4:c.886A=	ENSP00000341433.3:p.Met296=
NM_138691.2:c.886A=	NP_619636.2:p.Met296=
XM_011518213.1:c.1474A=	XP_011516515.1:p.Met492=
XM_017014256.1:c.889A=	XP_016869745.1:p.Met297=
NM_138691.3:c.886A= MANE Select	NP_619636.2:p.Met296=