Canonical Allele Identifier: CA350592680

Gene: WNT10A

Linked Data

• MyVariant Identifiers: chr2:g.219757958T>A (hg19) ; chr2:g.218893236T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218893236T>A , CM000664.2:g.218893236T>A	GRCh38
NC_000002.11:g.219757958T>A , CM000664.1:g.219757958T>A	GRCh37
NC_000002.10:g.219466202T>A	NCBI36
NG_012179.1:g.17704T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258411.8:c.1219T>A MANE Select	ENSP00000258411.3:p.Cys407Ser
ENST00000258411.7:c.1219T>A	ENSP00000258411.3:p.Cys407Ser
ENST00000489887.1:n.16T>A
NM_025216.2:c.1219T>A	NP_079492.2:p.Cys407Ser
XM_011511928.1:c.1168T>A	XP_011510230.1:p.Cys390Ser
XM_011511929.1:c.1123T>A	XP_011510231.1:p.Cys375Ser
XM_011511930.1:c.839T>A	XP_011510232.1:p.Val280Glu
XM_011511929.2:c.1123T>A	XP_011510231.1:p.Cys375Ser
NM_025216.3:c.1219T>A MANE Select	NP_079492.2:p.Cys407Ser