Canonical Allele Identifier: CA350592676

Gene: WNT10A

Linked Data

• gnomAD v4: 2-218893235-G-T
• MyVariant Identifiers: chr2:g.219757957G>T (hg19) ; chr2:g.218893235G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218893235G>T , CM000664.2:g.218893235G>T	GRCh38
NC_000002.11:g.219757957G>T , CM000664.1:g.219757957G>T	GRCh37
NC_000002.10:g.219466201G>T	NCBI36
NG_012179.1:g.17703G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258411.8:c.1218G>T MANE Select	ENSP00000258411.3:p.Glu406Asp
ENST00000258411.7:c.1218G>T	ENSP00000258411.3:p.Glu406Asp
ENST00000489887.1:n.15G>T
NM_025216.2:c.1218G>T	NP_079492.2:p.Glu406Asp
XM_011511928.1:c.1167G>T	XP_011510230.1:p.Glu389Asp
XM_011511929.1:c.1122G>T	XP_011510231.1:p.Glu374Asp
XM_011511930.1:c.838G>T	XP_011510232.1:p.Val280Leu
XM_011511929.2:c.1122G>T	XP_011510231.1:p.Glu374Asp
NM_025216.3:c.1218G>T MANE Select	NP_079492.2:p.Glu406Asp