Canonical Allele Identifier: CA1752365498

Gene: TMEM176A

Linked Data

• dbSNP Id: rs714885

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150802699T>G , CM000669.2:g.150802699T>G	GRCh38
NC_000007.13:g.150499787T>G , CM000669.1:g.150499787T>G	GRCh37
NC_000007.12:g.150130720T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000004103.8:c.285+374T>G MANE Select	ENSP00000004103.3:n.285+374T>G
ENST00000468689.2:c.108+374T>G	ENSP00000420081.2:n.108+374T>G
ENST00000004103.7:c.285+374T>G	ENSP00000004103.3:n.285+374T>G
ENST00000461345.5:c.108+374T>G	ENSP00000420818.1:n.108+374T>G
ENST00000462826.1:n.644T>G
ENST00000468689.1:c.108+374T>G	ENSP00000420081.1:n.108+374T>G
ENST00000475536.5:c.141+374T>G	ENSP00000417834.1:n.141+374T>G
ENST00000484928.5:c.285+374T>G	ENSP00000417626.1:n.285+374T>G
ENST00000494349.5:n.831+374T>G
NM_018487.2:c.285+374T>G	NP_060957.2:n.285+374T>G
XM_011516376.1:c.336+374T>G	XP_011514678.1:n.336+374T>G
XM_011516377.1:c.336+374T>G	XP_011514679.1:n.336+374T>G
XM_011516378.1:c.336+374T>G	XP_011514680.1:n.336+374T>G
XM_011516379.1:c.337-16T>G	XP_011514681.1:n.337-16T>G
XM_011516376.3:c.336+374T>G	XP_011514678.1:n.336+374T>G
XM_011516377.2:c.336+374T>G	XP_011514679.1:n.336+374T>G
XM_011516378.2:c.336+374T>G	XP_011514680.1:n.336+374T>G
XM_017012393.1:c.285+374T>G	XP_016867882.1:n.285+374T>G
XM_024446824.1:c.285+374T>G	XP_024302592.1:n.285+374T>G
NM_018487.3:c.285+374T>G MANE Select	NP_060957.2:n.285+374T>G