Canonical Allele Identifier: CA458642923

Gene: TMEM176A

Linked Data

• MyVariant Identifiers: chr7:g.150501485T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150804397T>C , CM000669.2:g.150804397T>C	GRCh38
NC_000007.13:g.150501485T>C , CM000669.1:g.150501485T>C	GRCh37
NC_000007.12:g.150132418T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000004103.8:c.591T>C MANE Select	ENSP00000004103.3:p.Gly197=
ENST00000468689.2:c.414T>C	ENSP00000420081.2:p.Gly138=
ENST00000004103.7:c.591T>C	ENSP00000004103.3:p.Gly197=
ENST00000461345.5:c.414T>C	ENSP00000420818.1:p.Gly138=
ENST00000462826.1:n.1778-430T>C
ENST00000474166.1:n.250T>C
ENST00000475007.5:n.487T>C
ENST00000475536.5:c.447T>C	ENSP00000417834.1:p.Gly149=
ENST00000481305.1:n.367-430T>C
ENST00000484928.5:c.591T>C	ENSP00000417626.1:p.Gly197=
ENST00000494349.5:n.1137T>C
NM_018487.2:c.591T>C	NP_060957.2:p.Gly197=
XM_011516376.1:c.642T>C	XP_011514678.1:p.Gly214=
XM_011516377.1:c.642T>C	XP_011514679.1:p.Gly214=
XM_011516378.1:c.607-430T>C	XP_011514680.1:n.607-430T>C
XM_011516376.3:c.642T>C	XP_011514678.1:p.Gly214=
XM_011516377.2:c.642T>C	XP_011514679.1:p.Gly214=
XM_011516378.2:c.607-430T>C	XP_011514680.1:n.607-430T>C
XM_017012393.1:c.591T>C	XP_016867882.1:p.Gly197=
XM_024446824.1:c.556-430T>C	XP_024302592.1:n.556-430T>C
NM_018487.3:c.591T>C MANE Select	NP_060957.2:p.Gly197=