Canonical Allele Identifier: CA1752367339

Gene: TMEM176A

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150804437T= , CM000669.2:g.150804437T=	GRCh38
NC_000007.13:g.150501525T= , CM000669.1:g.150501525T=	GRCh37
NC_000007.12:g.150132458T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000004103.8:c.631T= MANE Select	ENSP00000004103.3:p.Trp211=
ENST00000468689.2:c.454T=	ENSP00000420081.2:p.Trp152=
ENST00000004103.7:c.631T=	ENSP00000004103.3:p.Trp211=
ENST00000461345.5:c.454T=	ENSP00000420818.1:p.Trp152=
ENST00000462826.1:n.1778-390T=
ENST00000474166.1:n.290T=
ENST00000475007.5:n.527T=
ENST00000475536.5:c.487T=	ENSP00000417834.1:p.Trp163=
ENST00000481305.1:n.367-390T=
ENST00000484928.5:c.631T=	ENSP00000417626.1:p.Trp211=
ENST00000494349.5:n.1177T=
NM_018487.2:c.631T=	NP_060957.2:p.Trp211=
XM_011516376.1:c.682T=	XP_011514678.1:p.Trp228=
XM_011516377.1:c.682T=	XP_011514679.1:p.Trp228=
XM_011516378.1:c.607-390T=	XP_011514680.1:n.607-390T=
XM_011516376.3:c.682T=	XP_011514678.1:p.Trp228=
XM_011516377.2:c.682T=	XP_011514679.1:p.Trp228=
XM_011516378.2:c.607-390T=	XP_011514680.1:n.607-390T=
XM_017012393.1:c.631T=	XP_016867882.1:p.Trp211=
XM_024446824.1:c.556-390T=	XP_024302592.1:n.556-390T=
NM_018487.3:c.631T= MANE Select	NP_060957.2:p.Trp211=