Canonical Allele Identifier: CA369842993

Gene: TMEM176A

Linked Data

• MyVariant Identifiers: chr7:g.150501476G>A (hg19) ; chr7:g.150804388G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150804388G>A , CM000669.2:g.150804388G>A	GRCh38
NC_000007.13:g.150501476G>A , CM000669.1:g.150501476G>A	GRCh37
NC_000007.12:g.150132409G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000004103.8:c.582G>A MANE Select	ENSP00000004103.3:p.Met194Ile
ENST00000468689.2:c.405G>A	ENSP00000420081.2:p.Met135Ile
ENST00000004103.7:c.582G>A	ENSP00000004103.3:p.Met194Ile
ENST00000461345.5:c.405G>A	ENSP00000420818.1:p.Met135Ile
ENST00000462826.1:n.1778-439G>A
ENST00000474166.1:n.241G>A
ENST00000475007.5:n.478G>A
ENST00000475536.5:c.438G>A	ENSP00000417834.1:p.Met146Ile
ENST00000481305.1:n.367-439G>A
ENST00000484928.5:c.582G>A	ENSP00000417626.1:p.Met194Ile
ENST00000494349.5:n.1128G>A
NM_018487.2:c.582G>A	NP_060957.2:p.Met194Ile
XM_011516376.1:c.633G>A	XP_011514678.1:p.Met211Ile
XM_011516377.1:c.633G>A	XP_011514679.1:p.Met211Ile
XM_011516378.1:c.607-439G>A	XP_011514680.1:n.607-439G>A
XM_011516376.3:c.633G>A	XP_011514678.1:p.Met211Ile
XM_011516377.2:c.633G>A	XP_011514679.1:p.Met211Ile
XM_011516378.2:c.607-439G>A	XP_011514680.1:n.607-439G>A
XM_017012393.1:c.582G>A	XP_016867882.1:p.Met194Ile
XM_024446824.1:c.556-439G>A	XP_024302592.1:n.556-439G>A
NM_018487.3:c.582G>A MANE Select	NP_060957.2:p.Met194Ile