Canonical Allele Identifier: CA1855120660

Gene: TMC1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.72820898C= , CM000671.2:g.72820898C=	GRCh38
NC_000009.11:g.75435814C= , CM000671.1:g.75435814C=	GRCh37
NC_000009.10:g.74625634C=	NCBI36
NG_008213.1:g.304098C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000297784.10:c.1820C= MANE Select	ENSP00000297784.6:p.Thr607=
ENST00000644967.1:c.*260C=	ENSP00000496159.1:n.*260C=
ENST00000645053.1:c.1258-5971C=	ENSP00000493838.1:n.1258-5971C=
ENST00000645208.2:c.1820C=	ENSP00000494684.1:p.Thr607=
ENST00000645773.1:c.1694C=	ENSP00000493698.1:p.Thr565=
ENST00000645787.1:n.1963C=
ENST00000646619.1:c.1382C=	ENSP00000493726.1:p.Thr461=
ENST00000651183.1:c.1382C=	ENSP00000498723.1:p.Thr461=
ENST00000297784.9:c.1820C=	ENSP00000297784.5:p.Thr607=
ENST00000340019.4:c.1820C=	ENSP00000341433.3:p.Thr607=
ENST00000469455.1:n.301C=
ENST00000486417.5:n.718C=
NM_138691.2:c.1820C=	NP_619636.2:p.Thr607=
XM_011518213.1:c.2408C=	XP_011516515.1:p.Thr803=
XM_017014256.1:c.1823C=	XP_016869745.1:p.Thr608=
NM_138691.3:c.1820C= MANE Select	NP_619636.2:p.Thr607=