Canonical Allele Identifier: CA465492662

Gene: TMC1

Linked Data

• gnomAD v4: 9-72820950-C-G
• MyVariant Identifiers: chr9:g.75435866C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.72820950C>G , CM000671.2:g.72820950C>G	GRCh38
NC_000009.11:g.75435866C>G , CM000671.1:g.75435866C>G	GRCh37
NC_000009.10:g.74625686C>G	NCBI36
NG_008213.1:g.304150C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000297784.10:c.1872C>G MANE Select	ENSP00000297784.6:p.Ala624=
ENST00000644967.1:c.*312C>G	ENSP00000496159.1:n.*312C>G
ENST00000645053.1:c.1258-5919C>G	ENSP00000493838.1:n.1258-5919C>G
ENST00000645208.2:c.1872C>G	ENSP00000494684.1:p.Ala624=
ENST00000645773.1:c.1746C>G	ENSP00000493698.1:p.Ala582=
ENST00000645787.1:n.2015C>G
ENST00000646619.1:c.1434C>G	ENSP00000493726.1:p.Ala478=
ENST00000651183.1:c.1434C>G	ENSP00000498723.1:p.Ala478=
ENST00000297784.9:c.1872C>G	ENSP00000297784.5:p.Ala624=
ENST00000340019.4:c.1872C>G	ENSP00000341433.3:p.Ala624=
ENST00000469455.1:n.353C>G
ENST00000486417.5:n.770C>G
NM_138691.2:c.1872C>G	NP_619636.2:p.Ala624=
XM_011518213.1:c.2460C>G	XP_011516515.1:p.Ala820=
XM_017014256.1:c.1875C>G	XP_016869745.1:p.Ala625=
NM_138691.3:c.1872C>G MANE Select	NP_619636.2:p.Ala624=