Canonical Allele Identifier: CA373669709

Gene: TMC1

Linked Data

• dbSNP Id: rs932693448
• gnomAD v2: 9-75435841-T-G
• gnomAD v4: 9-72820925-T-G
• MyVariant Identifiers: chr9:g.75435841T>G (hg19) ; chr9:g.72820925T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.72820925T>G , CM000671.2:g.72820925T>G	GRCh38
NC_000009.11:g.75435841T>G , CM000671.1:g.75435841T>G	GRCh37
NC_000009.10:g.74625661T>G	NCBI36
NG_008213.1:g.304125T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000297784.10:c.1847T>G MANE Select	ENSP00000297784.6:p.Val616Gly
ENST00000644967.1:c.*287T>G	ENSP00000496159.1:n.*287T>G
ENST00000645053.1:c.1258-5944T>G	ENSP00000493838.1:n.1258-5944T>G
ENST00000645208.2:c.1847T>G	ENSP00000494684.1:p.Val616Gly
ENST00000645773.1:c.1721T>G	ENSP00000493698.1:p.Val574Gly
ENST00000645787.1:n.1990T>G
ENST00000646619.1:c.1409T>G	ENSP00000493726.1:p.Val470Gly
ENST00000651183.1:c.1409T>G	ENSP00000498723.1:p.Val470Gly
ENST00000297784.9:c.1847T>G	ENSP00000297784.5:p.Val616Gly
ENST00000340019.4:c.1847T>G	ENSP00000341433.3:p.Val616Gly
ENST00000469455.1:n.328T>G
ENST00000486417.5:n.745T>G
NM_138691.2:c.1847T>G	NP_619636.2:p.Val616Gly
XM_011518213.1:c.2435T>G	XP_011516515.1:p.Val812Gly
XM_017014256.1:c.1850T>G	XP_016869745.1:p.Val617Gly
NM_138691.3:c.1847T>G MANE Select	NP_619636.2:p.Val616Gly