Canonical Allele Identifier: CA1855120681

Gene: TMC1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.72820945G= , CM000671.2:g.72820945G=	GRCh38
NC_000009.11:g.75435861G= , CM000671.1:g.75435861G=	GRCh37
NC_000009.10:g.74625681G=	NCBI36
NG_008213.1:g.304145G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000297784.10:c.1867G= MANE Select	ENSP00000297784.6:p.Glu623=
ENST00000644967.1:c.*307G=	ENSP00000496159.1:n.*307G=
ENST00000645053.1:c.1258-5924G=	ENSP00000493838.1:n.1258-5924G=
ENST00000645208.2:c.1867G=	ENSP00000494684.1:p.Glu623=
ENST00000645773.1:c.1741G=	ENSP00000493698.1:p.Glu581=
ENST00000645787.1:n.2010G=
ENST00000646619.1:c.1429G=	ENSP00000493726.1:p.Glu477=
ENST00000651183.1:c.1429G=	ENSP00000498723.1:p.Glu477=
ENST00000297784.9:c.1867G=	ENSP00000297784.5:p.Glu623=
ENST00000340019.4:c.1867G=	ENSP00000341433.3:p.Glu623=
ENST00000469455.1:n.348G=
ENST00000486417.5:n.765G=
NM_138691.2:c.1867G=	NP_619636.2:p.Glu623=
XM_011518213.1:c.2455G=	XP_011516515.1:p.Glu819=
XM_017014256.1:c.1870G=	XP_016869745.1:p.Glu624=
NM_138691.3:c.1867G= MANE Select	NP_619636.2:p.Glu623=