Canonical Allele Identifier: CA1752367136

Gene: TMEM176A

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150804280C= , CM000669.2:g.150804280C=	GRCh38
NC_000007.13:g.150501368C= , CM000669.1:g.150501368C=	GRCh37
NC_000007.12:g.150132301C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000004103.8:c.556-82C= MANE Select	ENSP00000004103.3:n.556-82C=
ENST00000468689.2:c.379-82C=	ENSP00000420081.2:n.379-82C=
ENST00000004103.7:c.556-82C=	ENSP00000004103.3:n.556-82C=
ENST00000461345.5:c.379-82C=	ENSP00000420818.1:n.379-82C=
ENST00000462826.1:n.1777+448C=
ENST00000474166.1:n.215-82C=
ENST00000475007.5:n.452-82C=
ENST00000475536.5:c.412-82C=	ENSP00000417834.1:n.412-82C=
ENST00000481305.1:n.366+448C=
ENST00000484928.5:c.556-82C=	ENSP00000417626.1:n.556-82C=
ENST00000494349.5:n.1102-82C=
NM_018487.2:c.556-82C=	NP_060957.2:n.556-82C=
XM_011516376.1:c.607-82C=	XP_011514678.1:n.607-82C=
XM_011516377.1:c.607-82C=	XP_011514679.1:n.607-82C=
XM_011516378.1:c.606+448C=	XP_011514680.1:n.606+448C=
XM_011516376.3:c.607-82C=	XP_011514678.1:n.607-82C=
XM_011516377.2:c.607-82C=	XP_011514679.1:n.607-82C=
XM_011516378.2:c.606+448C=	XP_011514680.1:n.606+448C=
XM_017012393.1:c.556-82C=	XP_016867882.1:n.556-82C=
XM_024446824.1:c.555+448C=	XP_024302592.1:n.555+448C=
NM_018487.3:c.556-82C= MANE Select	NP_060957.2:n.556-82C=