Canonical Allele Identifier: CA373670175

Gene: TMC1

Linked Data

• gnomAD v4: 9-72821020-A-G
• MyVariant Identifiers: chr9:g.75435936A>G (hg19) ; chr9:g.72821020A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.72821020A>G , CM000671.2:g.72821020A>G	GRCh38
NC_000009.11:g.75435936A>G , CM000671.1:g.75435936A>G	GRCh37
NC_000009.10:g.74625756A>G	NCBI36
NG_008213.1:g.304220A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000297784.10:c.1942A>G MANE Select	ENSP00000297784.6:p.Thr648Ala
ENST00000644967.1:c.*382A>G	ENSP00000496159.1:n.*382A>G
ENST00000645053.1:c.1258-5849A>G	ENSP00000493838.1:n.1258-5849A>G
ENST00000645208.2:c.1942A>G	ENSP00000494684.1:p.Thr648Ala
ENST00000645773.1:c.1816A>G	ENSP00000493698.1:p.Thr606Ala
ENST00000645787.1:n.2085A>G
ENST00000646619.1:c.1504A>G	ENSP00000493726.1:p.Thr502Ala
ENST00000651183.1:c.1504A>G	ENSP00000498723.1:p.Thr502Ala
ENST00000297784.9:c.1942A>G	ENSP00000297784.5:p.Thr648Ala
ENST00000340019.4:c.1942A>G	ENSP00000341433.3:p.Thr648Ala
ENST00000469455.1:n.423A>G
ENST00000486417.5:n.840A>G
NM_138691.2:c.1942A>G	NP_619636.2:p.Thr648Ala
XM_011518213.1:c.2530A>G	XP_011516515.1:p.Thr844Ala
XM_017014256.1:c.1945A>G	XP_016869745.1:p.Thr649Ala
NM_138691.3:c.1942A>G MANE Select	NP_619636.2:p.Thr648Ala