Canonical Allele Identifier: CA350592780

Gene: WNT10A

Linked Data

• MyVariant Identifiers: chr2:g.219757973T>G (hg19) ; chr2:g.218893251T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218893251T>G , CM000664.2:g.218893251T>G	GRCh38
NC_000002.11:g.219757973T>G , CM000664.1:g.219757973T>G	GRCh37
NC_000002.10:g.219466217T>G	NCBI36
NG_012179.1:g.17719T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258411.8:c.1234T>G MANE Select	ENSP00000258411.3:p.Trp412Gly
ENST00000258411.7:c.1234T>G	ENSP00000258411.3:p.Trp412Gly
ENST00000489887.1:n.31T>G
NM_025216.2:c.1234T>G	NP_079492.2:p.Trp412Gly
XM_011511928.1:c.1183T>G	XP_011510230.1:p.Trp395Gly
XM_011511929.1:c.1138T>G	XP_011510231.1:p.Trp380Gly
XM_011511930.1:c.854T>G	XP_011510232.1:p.Val285Gly
XM_011511929.2:c.1138T>G	XP_011510231.1:p.Trp380Gly
NM_025216.3:c.1234T>G MANE Select	NP_079492.2:p.Trp412Gly