Canonical Allele Identifier: CA373669814

Gene: TMC1

Linked Data

• MyVariant Identifiers: chr9:g.75435891A>C (hg19) ; chr9:g.72820975A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.72820975A>C , CM000671.2:g.72820975A>C	GRCh38
NC_000009.11:g.75435891A>C , CM000671.1:g.75435891A>C	GRCh37
NC_000009.10:g.74625711A>C	NCBI36
NG_008213.1:g.304175A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000297784.10:c.1897A>C MANE Select	ENSP00000297784.6:p.Asn633His
ENST00000644967.1:c.*337A>C	ENSP00000496159.1:n.*337A>C
ENST00000645053.1:c.1258-5894A>C	ENSP00000493838.1:n.1258-5894A>C
ENST00000645208.2:c.1897A>C	ENSP00000494684.1:p.Asn633His
ENST00000645773.1:c.1771A>C	ENSP00000493698.1:p.Asn591His
ENST00000645787.1:n.2040A>C
ENST00000646619.1:c.1459A>C	ENSP00000493726.1:p.Asn487His
ENST00000651183.1:c.1459A>C	ENSP00000498723.1:p.Asn487His
ENST00000297784.9:c.1897A>C	ENSP00000297784.5:p.Asn633His
ENST00000340019.4:c.1897A>C	ENSP00000341433.3:p.Asn633His
ENST00000469455.1:n.378A>C
ENST00000486417.5:n.795A>C
NM_138691.2:c.1897A>C	NP_619636.2:p.Asn633His
XM_011518213.1:c.2485A>C	XP_011516515.1:p.Asn829His
XM_017014256.1:c.1900A>C	XP_016869745.1:p.Asn634His
NM_138691.3:c.1897A>C MANE Select	NP_619636.2:p.Asn633His