Canonical Allele Identifier: CA373668489

Gene: TMC1

Linked Data

• MyVariant Identifiers: chr9:g.75431124C>G (hg19) ; chr9:g.72816208C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.72816208C>G , CM000671.2:g.72816208C>G	GRCh38
NC_000009.11:g.75431124C>G , CM000671.1:g.75431124C>G	GRCh37
NC_000009.10:g.74620944C>G	NCBI36
NG_008213.1:g.299408C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000297784.10:c.1761C>G MANE Select	ENSP00000297784.6:p.Ile587Met
ENST00000644967.1:c.1323C>G	ENSP00000496159.1:p.Ile441Met
ENST00000645053.1:c.1258-10661C>G	ENSP00000493838.1:n.1258-10661C>G
ENST00000645208.2:c.1761C>G	ENSP00000494684.1:p.Ile587Met
ENST00000645773.1:c.1635C>G	ENSP00000493698.1:p.Ile545Met
ENST00000645787.1:n.1904C>G
ENST00000646619.1:c.1323C>G	ENSP00000493726.1:p.Ile441Met
ENST00000651183.1:c.1323C>G	ENSP00000498723.1:p.Ile441Met
ENST00000297784.9:c.1761C>G	ENSP00000297784.5:p.Ile587Met
ENST00000340019.4:c.1761C>G	ENSP00000341433.3:p.Ile587Met
ENST00000469455.1:n.242C>G
ENST00000486417.5:n.385C>G
NM_138691.2:c.1761C>G	NP_619636.2:p.Ile587Met
XM_011518213.1:c.2349C>G	XP_011516515.1:p.Ile783Met
XM_017014256.1:c.1764C>G	XP_016869745.1:p.Ile588Met
NM_138691.3:c.1761C>G MANE Select	NP_619636.2:p.Ile587Met