Canonical Allele Identifier: CA1855120844

Gene: TMC1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.72821272T= , CM000671.2:g.72821272T=	GRCh38
NC_000009.11:g.75436188T= , CM000671.1:g.75436188T=	GRCh37
NC_000009.10:g.74626008T=	NCBI36
NG_008213.1:g.304472T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000297784.10:c.2003+191T= MANE Select	ENSP00000297784.6:n.2003+191T=
ENST00000644967.1:c.*443+191T=	ENSP00000496159.1:n.*443+191T=
ENST00000645053.1:c.1258-5597T=	ENSP00000493838.1:n.1258-5597T=
ENST00000645208.2:c.2003+191T=	ENSP00000494684.1:n.2003+191T=
ENST00000645773.1:c.1877+191T=	ENSP00000493698.1:n.1877+191T=
ENST00000645787.1:n.2146+191T=
ENST00000646619.1:c.1565+191T=	ENSP00000493726.1:n.1565+191T=
ENST00000651183.1:c.1565+191T=	ENSP00000498723.1:n.1565+191T=
ENST00000297784.9:c.2003+191T=	ENSP00000297784.5:n.2003+191T=
ENST00000340019.4:c.2003+191T=	ENSP00000341433.3:n.2003+191T=
ENST00000469455.1:n.484+191T=
ENST00000486417.5:n.901+191T=
NM_138691.2:c.2003+191T=	NP_619636.2:n.2003+191T=
XM_011518213.1:c.2591+191T=	XP_011516515.1:n.2591+191T=
XM_017014256.1:c.2006+191T=	XP_016869745.1:n.2006+191T=
NM_138691.3:c.2003+191T= MANE Select	NP_619636.2:n.2003+191T=