Canonical Allele Identifier: CA1855068088

Gene: TMC1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.72700596T= , CM000671.2:g.72700596T=	GRCh38
NC_000009.11:g.75315512T= , CM000671.1:g.75315512T=	GRCh37
NC_000009.10:g.74505332T=	NCBI36
NG_008213.1:g.183796T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000297784.10:c.315T= MANE Select	ENSP00000297784.6:p.Thr105=
ENST00000644967.1:c.-77+5882T=	ENSP00000496159.1:n.-77+5882T=
ENST00000645053.1:c.-77+5882T=	ENSP00000493838.1:n.-77+5882T=
ENST00000645208.2:c.315T=	ENSP00000494684.1:p.Thr105=
ENST00000645773.1:c.236+5882T=	ENSP00000493698.1:n.236+5882T=
ENST00000645787.1:n.355T=
ENST00000646244.1:n.765T=
ENST00000646619.1:c.-77+5882T=	ENSP00000493726.1:n.-77+5882T=
ENST00000650689.1:n.660+5882T=
ENST00000651183.1:c.-77+5882T=	ENSP00000498723.1:n.-77+5882T=
ENST00000297784.9:c.315T=	ENSP00000297784.5:p.Thr105=
ENST00000340019.4:c.315T=	ENSP00000341433.3:p.Thr105=
NM_138691.2:c.315T=	NP_619636.2:p.Thr105=
XM_011518213.1:c.903T=	XP_011516515.1:p.Thr301=
XM_017014256.1:c.318T=	XP_016869745.1:p.Thr106=
NM_138691.3:c.315T= MANE Select	NP_619636.2:p.Thr105=