Canonical Allele Identifier: CA369842951

Gene: TMEM176A

Linked Data

• MyVariant Identifiers: chr7:g.150501457T>A (hg19) ; chr7:g.150804369T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150804369T>A , CM000669.2:g.150804369T>A	GRCh38
NC_000007.13:g.150501457T>A , CM000669.1:g.150501457T>A	GRCh37
NC_000007.12:g.150132390T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000004103.8:c.563T>A MANE Select	ENSP00000004103.3:p.Phe188Tyr
ENST00000468689.2:c.386T>A	ENSP00000420081.2:p.Phe129Tyr
ENST00000004103.7:c.563T>A	ENSP00000004103.3:p.Phe188Tyr
ENST00000461345.5:c.386T>A	ENSP00000420818.1:p.Phe129Tyr
ENST00000462826.1:n.1778-458T>A
ENST00000474166.1:n.222T>A
ENST00000475007.5:n.459T>A
ENST00000475536.5:c.419T>A	ENSP00000417834.1:p.Phe140Tyr
ENST00000481305.1:n.367-458T>A
ENST00000484928.5:c.563T>A	ENSP00000417626.1:p.Phe188Tyr
ENST00000494349.5:n.1109T>A
NM_018487.2:c.563T>A	NP_060957.2:p.Phe188Tyr
XM_011516376.1:c.614T>A	XP_011514678.1:p.Phe205Tyr
XM_011516377.1:c.614T>A	XP_011514679.1:p.Phe205Tyr
XM_011516378.1:c.607-458T>A	XP_011514680.1:n.607-458T>A
XM_011516376.3:c.614T>A	XP_011514678.1:p.Phe205Tyr
XM_011516377.2:c.614T>A	XP_011514679.1:p.Phe205Tyr
XM_011516378.2:c.607-458T>A	XP_011514680.1:n.607-458T>A
XM_017012393.1:c.563T>A	XP_016867882.1:p.Phe188Tyr
XM_024446824.1:c.556-458T>A	XP_024302592.1:n.556-458T>A
NM_018487.3:c.563T>A MANE Select	NP_060957.2:p.Phe188Tyr