Canonical Allele Identifier: CA1752367227

Gene: TMEM176A

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000004103.8:c.556G= MANE Select	ENSP00000004103.3:p.Ala186=
ENST00000468689.2:c.379G=	ENSP00000420081.2:p.Ala127=
ENST00000004103.7:c.556G=	ENSP00000004103.3:p.Ala186=
ENST00000461345.5:c.379G=	ENSP00000420818.1:p.Ala127=
ENST00000462826.1:n.1778-465G=
ENST00000474166.1:n.215G=
ENST00000475007.5:n.452G=
ENST00000475536.5:c.412G=	ENSP00000417834.1:p.Ala138=
ENST00000481305.1:n.367-465G=
ENST00000484928.5:c.556G=	ENSP00000417626.1:p.Ala186=
ENST00000494349.5:n.1102G=
NM_018487.2:c.556G=	NP_060957.2:p.Ala186=
XM_011516376.1:c.607G=	XP_011514678.1:p.Ala203=
XM_011516377.1:c.607G=	XP_011514679.1:p.Ala203=
XM_011516378.1:c.607-465G=	XP_011514680.1:n.607-465G=
XM_011516376.3:c.607G=	XP_011514678.1:p.Ala203=
XM_011516377.2:c.607G=	XP_011514679.1:p.Ala203=
XM_011516378.2:c.607-465G=	XP_011514680.1:n.607-465G=
XM_017012393.1:c.556G=	XP_016867882.1:p.Ala186=
XM_024446824.1:c.556-465G=	XP_024302592.1:n.556-465G=
NM_018487.3:c.556G= MANE Select	NP_060957.2:p.Ala186=