Canonical Allele Identifier: CA369842936

Gene: TMEM176A

Linked Data

• dbSNP Id: rs1798877031
• gnomAD v4: 7-150804362-G-A
• MyVariant Identifiers: chr7:g.150501450G>A (hg19) ; chr7:g.150804362G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150804362G>A , CM000669.2:g.150804362G>A	GRCh38
NC_000007.13:g.150501450G>A , CM000669.1:g.150501450G>A	GRCh37
NC_000007.12:g.150132383G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000004103.8:c.556G>A MANE Select	ENSP00000004103.3:p.Ala186Thr
ENST00000468689.2:c.379G>A	ENSP00000420081.2:p.Ala127Thr
ENST00000004103.7:c.556G>A	ENSP00000004103.3:p.Ala186Thr
ENST00000461345.5:c.379G>A	ENSP00000420818.1:p.Ala127Thr
ENST00000462826.1:n.1778-465G>A
ENST00000474166.1:n.215G>A
ENST00000475007.5:n.452G>A
ENST00000475536.5:c.412G>A	ENSP00000417834.1:p.Ala138Thr
ENST00000481305.1:n.367-465G>A
ENST00000484928.5:c.556G>A	ENSP00000417626.1:p.Ala186Thr
ENST00000494349.5:n.1102G>A
NM_018487.2:c.556G>A	NP_060957.2:p.Ala186Thr
XM_011516376.1:c.607G>A	XP_011514678.1:p.Ala203Thr
XM_011516377.1:c.607G>A	XP_011514679.1:p.Ala203Thr
XM_011516378.1:c.607-465G>A	XP_011514680.1:n.607-465G>A
XM_011516376.3:c.607G>A	XP_011514678.1:p.Ala203Thr
XM_011516377.2:c.607G>A	XP_011514679.1:p.Ala203Thr
XM_011516378.2:c.607-465G>A	XP_011514680.1:n.607-465G>A
XM_017012393.1:c.556G>A	XP_016867882.1:p.Ala186Thr
XM_024446824.1:c.556-465G>A	XP_024302592.1:n.556-465G>A
NM_018487.3:c.556G>A MANE Select	NP_060957.2:p.Ala186Thr