Canonical Allele Identifier: CA1855118680

Gene: TMC1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.72816192T= , CM000671.2:g.72816192T=	GRCh38
NC_000009.11:g.75431108T= , CM000671.1:g.75431108T=	GRCh37
NC_000009.10:g.74620928T=	NCBI36
NG_008213.1:g.299392T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000297784.10:c.1745T= MANE Select	ENSP00000297784.6:p.Phe582=
ENST00000644967.1:c.1307T=	ENSP00000496159.1:p.Phe436=
ENST00000645053.1:c.1258-10677T=	ENSP00000493838.1:n.1258-10677T=
ENST00000645208.2:c.1745T=	ENSP00000494684.1:p.Phe582=
ENST00000645773.1:c.1619T=	ENSP00000493698.1:p.Phe540=
ENST00000645787.1:n.1888T=
ENST00000646619.1:c.1307T=	ENSP00000493726.1:p.Phe436=
ENST00000651183.1:c.1307T=	ENSP00000498723.1:p.Phe436=
ENST00000297784.9:c.1745T=	ENSP00000297784.5:p.Phe582=
ENST00000340019.4:c.1745T=	ENSP00000341433.3:p.Phe582=
ENST00000469455.1:n.226T=
ENST00000486417.5:n.369T=
NM_138691.2:c.1745T=	NP_619636.2:p.Phe582=
XM_011518213.1:c.2333T=	XP_011516515.1:p.Phe778=
XM_017014256.1:c.1748T=	XP_016869745.1:p.Phe583=
NM_138691.3:c.1745T= MANE Select	NP_619636.2:p.Phe582=