Canonical Allele Identifier: CA458642925

Gene: TMEM176A

Linked Data

• MyVariant Identifiers: chr7:g.150501488C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150804400C>A , CM000669.2:g.150804400C>A	GRCh38
NC_000007.13:g.150501488C>A , CM000669.1:g.150501488C>A	GRCh37
NC_000007.12:g.150132421C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000004103.8:c.594C>A MANE Select	ENSP00000004103.3:p.Val198=
ENST00000468689.2:c.417C>A	ENSP00000420081.2:p.Val139=
ENST00000004103.7:c.594C>A	ENSP00000004103.3:p.Val198=
ENST00000461345.5:c.417C>A	ENSP00000420818.1:p.Val139=
ENST00000462826.1:n.1778-427C>A
ENST00000474166.1:n.253C>A
ENST00000475007.5:n.490C>A
ENST00000475536.5:c.450C>A	ENSP00000417834.1:p.Val150=
ENST00000481305.1:n.367-427C>A
ENST00000484928.5:c.594C>A	ENSP00000417626.1:p.Val198=
ENST00000494349.5:n.1140C>A
NM_018487.2:c.594C>A	NP_060957.2:p.Val198=
XM_011516376.1:c.645C>A	XP_011514678.1:p.Val215=
XM_011516377.1:c.645C>A	XP_011514679.1:p.Val215=
XM_011516378.1:c.607-427C>A	XP_011514680.1:n.607-427C>A
XM_011516376.3:c.645C>A	XP_011514678.1:p.Val215=
XM_011516377.2:c.645C>A	XP_011514679.1:p.Val215=
XM_011516378.2:c.607-427C>A	XP_011514680.1:n.607-427C>A
XM_017012393.1:c.594C>A	XP_016867882.1:p.Val198=
XM_024446824.1:c.556-427C>A	XP_024302592.1:n.556-427C>A
NM_018487.3:c.594C>A MANE Select	NP_060957.2:p.Val198=