Canonical Allele Identifier: CA1855068082

Gene: TMC1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.72700575G= , CM000671.2:g.72700575G=	GRCh38
NC_000009.11:g.75315491G= , CM000671.1:g.75315491G=	GRCh37
NC_000009.10:g.74505311G=	NCBI36
NG_008213.1:g.183775G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000297784.10:c.294G= MANE Select	ENSP00000297784.6:p.Glu98=
ENST00000644967.1:c.-77+5861G=	ENSP00000496159.1:n.-77+5861G=
ENST00000645053.1:c.-77+5861G=	ENSP00000493838.1:n.-77+5861G=
ENST00000645208.2:c.294G=	ENSP00000494684.1:p.Glu98=
ENST00000645773.1:c.236+5861G=	ENSP00000493698.1:n.236+5861G=
ENST00000645787.1:n.334G=
ENST00000646244.1:n.744G=
ENST00000646619.1:c.-77+5861G=	ENSP00000493726.1:n.-77+5861G=
ENST00000650689.1:n.660+5861G=
ENST00000651183.1:c.-77+5861G=	ENSP00000498723.1:n.-77+5861G=
ENST00000297784.9:c.294G=	ENSP00000297784.5:p.Glu98=
ENST00000340019.4:c.294G=	ENSP00000341433.3:p.Glu98=
NM_138691.2:c.294G=	NP_619636.2:p.Glu98=
XM_011518213.1:c.882G=	XP_011516515.1:p.Glu294=
XM_017014256.1:c.297G=	XP_016869745.1:p.Glu99=
NM_138691.3:c.294G= MANE Select	NP_619636.2:p.Glu98=