Canonical Allele Identifier: CA350592747

Gene: WNT10A

Linked Data

• MyVariant Identifiers: chr2:g.219757966C>G (hg19) ; chr2:g.218893244C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218893244C>G , CM000664.2:g.218893244C>G	GRCh38
NC_000002.11:g.219757966C>G , CM000664.1:g.219757966C>G	GRCh37
NC_000002.10:g.219466210C>G	NCBI36
NG_012179.1:g.17712C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258411.8:c.1227C>G MANE Select	ENSP00000258411.3:p.Ile409Met
ENST00000258411.7:c.1227C>G	ENSP00000258411.3:p.Ile409Met
ENST00000489887.1:n.24C>G
NM_025216.2:c.1227C>G	NP_079492.2:p.Ile409Met
XM_011511928.1:c.1176C>G	XP_011510230.1:p.Ile392Met
XM_011511929.1:c.1131C>G	XP_011510231.1:p.Ile377Met
XM_011511930.1:c.847C>G	XP_011510232.1:p.His283Asp
XM_011511929.2:c.1131C>G	XP_011510231.1:p.Ile377Met
NM_025216.3:c.1227C>G MANE Select	NP_079492.2:p.Ile409Met