Canonical Allele Identifier: CA1752367244

Gene: TMEM176A

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150804375C= , CM000669.2:g.150804375C=	GRCh38
NC_000007.13:g.150501463C= , CM000669.1:g.150501463C=	GRCh37
NC_000007.12:g.150132396C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000004103.8:c.569C= MANE Select	ENSP00000004103.3:p.Thr190=
ENST00000468689.2:c.392C=	ENSP00000420081.2:p.Thr131=
ENST00000004103.7:c.569C=	ENSP00000004103.3:p.Thr190=
ENST00000461345.5:c.392C=	ENSP00000420818.1:p.Thr131=
ENST00000462826.1:n.1778-452C=
ENST00000474166.1:n.228C=
ENST00000475007.5:n.465C=
ENST00000475536.5:c.425C=	ENSP00000417834.1:p.Thr142=
ENST00000481305.1:n.367-452C=
ENST00000484928.5:c.569C=	ENSP00000417626.1:p.Thr190=
ENST00000494349.5:n.1115C=
NM_018487.2:c.569C=	NP_060957.2:p.Thr190=
XM_011516376.1:c.620C=	XP_011514678.1:p.Thr207=
XM_011516377.1:c.620C=	XP_011514679.1:p.Thr207=
XM_011516378.1:c.607-452C=	XP_011514680.1:n.607-452C=
XM_011516376.3:c.620C=	XP_011514678.1:p.Thr207=
XM_011516377.2:c.620C=	XP_011514679.1:p.Thr207=
XM_011516378.2:c.607-452C=	XP_011514680.1:n.607-452C=
XM_017012393.1:c.569C=	XP_016867882.1:p.Thr190=
XM_024446824.1:c.556-452C=	XP_024302592.1:n.556-452C=
NM_018487.3:c.569C= MANE Select	NP_060957.2:p.Thr190=