Canonical Allele Identifier: CA458642959

Gene: TMEM176A

Linked Data

• MyVariant Identifiers: chr7:g.150501521T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150804433T>A , CM000669.2:g.150804433T>A	GRCh38
NC_000007.13:g.150501521T>A , CM000669.1:g.150501521T>A	GRCh37
NC_000007.12:g.150132454T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000004103.8:c.627T>A MANE Select	ENSP00000004103.3:p.Pro209=
ENST00000468689.2:c.450T>A	ENSP00000420081.2:p.Pro150=
ENST00000004103.7:c.627T>A	ENSP00000004103.3:p.Pro209=
ENST00000461345.5:c.450T>A	ENSP00000420818.1:p.Pro150=
ENST00000462826.1:n.1778-394T>A
ENST00000474166.1:n.286T>A
ENST00000475007.5:n.523T>A
ENST00000475536.5:c.483T>A	ENSP00000417834.1:p.Pro161=
ENST00000481305.1:n.367-394T>A
ENST00000484928.5:c.627T>A	ENSP00000417626.1:p.Pro209=
ENST00000494349.5:n.1173T>A
NM_018487.2:c.627T>A	NP_060957.2:p.Pro209=
XM_011516376.1:c.678T>A	XP_011514678.1:p.Pro226=
XM_011516377.1:c.678T>A	XP_011514679.1:p.Pro226=
XM_011516378.1:c.607-394T>A	XP_011514680.1:n.607-394T>A
XM_011516376.3:c.678T>A	XP_011514678.1:p.Pro226=
XM_011516377.2:c.678T>A	XP_011514679.1:p.Pro226=
XM_011516378.2:c.607-394T>A	XP_011514680.1:n.607-394T>A
XM_017012393.1:c.627T>A	XP_016867882.1:p.Pro209=
XM_024446824.1:c.556-394T>A	XP_024302592.1:n.556-394T>A
NM_018487.3:c.627T>A MANE Select	NP_060957.2:p.Pro209=