Canonical Allele Identifier: CA1855118648

Gene: TMC1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.72816121A= , CM000671.2:g.72816121A=	GRCh38
NC_000009.11:g.75431037A= , CM000671.1:g.75431037A=	GRCh37
NC_000009.10:g.74620857A=	NCBI36
NG_008213.1:g.299321A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000297784.10:c.1696-22A= MANE Select	ENSP00000297784.6:n.1696-22A=
ENST00000644967.1:c.1258-22A=	ENSP00000496159.1:n.1258-22A=
ENST00000645053.1:c.1257+10611A=	ENSP00000493838.1:n.1257+10611A=
ENST00000645208.2:c.1696-22A=	ENSP00000494684.1:n.1696-22A=
ENST00000645773.1:c.1570-22A=	ENSP00000493698.1:n.1570-22A=
ENST00000645787.1:n.1839-22A=
ENST00000646619.1:c.1258-22A=	ENSP00000493726.1:n.1258-22A=
ENST00000651183.1:c.1258-22A=	ENSP00000498723.1:n.1258-22A=
ENST00000297784.9:c.1696-22A=	ENSP00000297784.5:n.1696-22A=
ENST00000340019.4:c.1696-22A=	ENSP00000341433.3:n.1696-22A=
ENST00000469455.1:n.177-22A=
ENST00000486417.5:n.320-22A=
NM_138691.2:c.1696-22A=	NP_619636.2:n.1696-22A=
XM_011518213.1:c.2284-22A=	XP_011516515.1:n.2284-22A=
XM_017014256.1:c.1699-22A=	XP_016869745.1:n.1699-22A=
NM_138691.3:c.1696-22A= MANE Select	NP_619636.2:n.1696-22A=