Canonical Allele Identifier: CA1855105902

Gene: TMC1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.72788253C= , CM000671.2:g.72788253C=	GRCh38
NC_000009.11:g.75403169C= , CM000671.1:g.75403169C=	GRCh37
NC_000009.10:g.74592989C=	NCBI36
NG_008213.1:g.271453C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000297784.10:c.885-86C= MANE Select	ENSP00000297784.6:n.885-86C=
ENST00000644967.1:c.447-86C=	ENSP00000496159.1:n.447-86C=
ENST00000645053.1:c.447-86C=	ENSP00000493838.1:n.447-86C=
ENST00000645208.2:c.885-86C=	ENSP00000494684.1:n.885-86C=
ENST00000645773.1:c.759-86C=	ENSP00000493698.1:n.759-86C=
ENST00000645787.1:n.925-86C=
ENST00000646619.1:c.447-86C=	ENSP00000493726.1:n.447-86C=
ENST00000650689.1:n.1183-86C=
ENST00000651183.1:c.447-86C=	ENSP00000498723.1:n.447-86C=
ENST00000297784.9:c.885-86C=	ENSP00000297784.5:n.885-86C=
ENST00000340019.4:c.885-86C=	ENSP00000341433.3:n.885-86C=
NM_138691.2:c.885-86C=	NP_619636.2:n.885-86C=
XM_011518213.1:c.1473-86C=	XP_011516515.1:n.1473-86C=
XM_017014256.1:c.888-86C=	XP_016869745.1:n.888-86C=
NM_138691.3:c.885-86C= MANE Select	NP_619636.2:n.885-86C=