Canonical Allele Identifier: CA350618286

Gene: WNT10A

Linked Data

• dbSNP Id: rs1425958867
• gnomAD v2: 2-219746939-C-T
• gnomAD v4: 2-218882217-C-T
• MyVariant Identifiers: chr2:g.219746939C>T (hg19) ; chr2:g.218882217C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218882217C>T , CM000664.2:g.218882217C>T	GRCh38
NC_000002.11:g.219746939C>T , CM000664.1:g.219746939C>T	GRCh37
NC_000002.10:g.219455183C>T	NCBI36
NG_012179.1:g.6685C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258411.8:c.170C>T MANE Select	ENSP00000258411.3:p.Ala57Val
ENST00000258411.7:c.170C>T	ENSP00000258411.3:p.Ala57Val
ENST00000458582.1:c.57C>T
NM_025216.2:c.170C>T	NP_079492.2:p.Ala57Val
XM_011511928.1:c.119C>T	XP_011510230.1:p.Ala40Val
XM_011511929.1:c.74C>T	XP_011510231.1:p.Ala25Val
XM_011511930.1:c.170C>T	XP_011510232.1:p.Ala57Val
XM_011511929.2:c.74C>T	XP_011510231.1:p.Ala25Val
NM_025216.3:c.170C>T MANE Select	NP_079492.2:p.Ala57Val