Canonical Allele Identifier: CA350586994

Gene: WNT10A

Linked Data

• MyVariant Identifiers: chr2:g.219754984G>A (hg19) ; chr2:g.218890262G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218890262G>A , CM000664.2:g.218890262G>A	GRCh38
NC_000002.11:g.219754984G>A , CM000664.1:g.219754984G>A	GRCh37
NC_000002.10:g.219463228G>A	NCBI36
NG_012179.1:g.14730G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000258411.8:c.655G>A MANE Select	ENSP00000258411.3:p.Gly219Ser
ENST00000258411.7:c.655G>A	ENSP00000258411.3:p.Gly219Ser
ENST00000458582.1:c.264-2512G>A
NM_025216.2:c.655G>A	NP_079492.2:p.Gly219Ser
XM_011511928.1:c.604G>A	XP_011510230.1:p.Gly202Ser
XM_011511929.1:c.559G>A	XP_011510231.1:p.Gly187Ser
XM_011511930.1:c.377-2512G>A	XP_011510232.1:n.377-2512G>A
XM_011511929.2:c.559G>A	XP_011510231.1:p.Gly187Ser
NM_025216.3:c.655G>A MANE Select	NP_079492.2:p.Gly219Ser