Canonical Allele Identifier: CA350592915

Gene: WNT10A

Linked Data

• MyVariant Identifiers: chr2:g.219757991T>G (hg19) ; chr2:g.218893269T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218893269T>G , CM000664.2:g.218893269T>G	GRCh38
NC_000002.11:g.219757991T>G , CM000664.1:g.219757991T>G	GRCh37
NC_000002.10:g.219466235T>G	NCBI36
NG_012179.1:g.17737T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258411.8:c.1252T>G MANE Select	ENSP00000258411.3:p.Ter418Gly
ENST00000258411.7:c.1252T>G	ENSP00000258411.3:p.Ter418Gly
ENST00000489887.1:n.47+2T>G
NM_025216.2:c.1252T>G	NP_079492.2:p.Ter418Gly
XM_011511928.1:c.1201T>G	XP_011510230.1:p.Ter401Gly
XM_011511929.1:c.1156T>G	XP_011510231.1:p.Ter386Gly
XM_011511930.1:c.872T>G	XP_011510232.1:p.Val291Gly
XM_011511929.2:c.1156T>G	XP_011510231.1:p.Ter386Gly
NM_025216.3:c.1252T>G MANE Select	NP_079492.2:p.Ter418Gly