Canonical Allele Identifier: CA465492606

Gene: TMC1

Linked Data

• MyVariant Identifiers: chr9:g.75435776T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.72820860T>G , CM000671.2:g.72820860T>G	GRCh38
NC_000009.11:g.75435776T>G , CM000671.1:g.75435776T>G	GRCh37
NC_000009.10:g.74625596T>G	NCBI36
NG_008213.1:g.304060T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000297784.10:c.1782T>G MANE Select	ENSP00000297784.6:p.Ala594=
ENST00000644967.1:c.*222T>G	ENSP00000496159.1:n.*222T>G
ENST00000645053.1:c.1258-6009T>G	ENSP00000493838.1:n.1258-6009T>G
ENST00000645208.2:c.1782T>G	ENSP00000494684.1:p.Ala594=
ENST00000645773.1:c.1656T>G	ENSP00000493698.1:p.Ala552=
ENST00000645787.1:n.1925T>G
ENST00000646619.1:c.1344T>G	ENSP00000493726.1:p.Ala448=
ENST00000651183.1:c.1344T>G	ENSP00000498723.1:p.Ala448=
ENST00000297784.9:c.1782T>G	ENSP00000297784.5:p.Ala594=
ENST00000340019.4:c.1782T>G	ENSP00000341433.3:p.Ala594=
ENST00000469455.1:n.263T>G
ENST00000486417.5:n.680T>G
NM_138691.2:c.1782T>G	NP_619636.2:p.Ala594=
XM_011518213.1:c.2370T>G	XP_011516515.1:p.Ala790=
XM_017014256.1:c.1785T>G	XP_016869745.1:p.Ala595=
NM_138691.3:c.1782T>G MANE Select	NP_619636.2:p.Ala594=