Canonical Allele Identifier: CA350592531

Gene: WNT10A

Linked Data

• dbSNP Id: rs1944679095
• gnomAD v3: 2-218893219-T-G
• gnomAD v4: 2-218893219-T-G
• MyVariant Identifiers: chr2:g.219757941T>G (hg19) ; chr2:g.218893219T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218893219T>G , CM000664.2:g.218893219T>G	GRCh38
NC_000002.11:g.219757941T>G , CM000664.1:g.219757941T>G	GRCh37
NC_000002.10:g.219466185T>G	NCBI36
NG_012179.1:g.17687T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258411.8:c.1202T>G MANE Select	ENSP00000258411.3:p.Phe401Cys
ENST00000258411.7:c.1202T>G	ENSP00000258411.3:p.Phe401Cys
NM_025216.2:c.1202T>G	NP_079492.2:p.Phe401Cys
XM_011511928.1:c.1151T>G	XP_011510230.1:p.Phe384Cys
XM_011511929.1:c.1106T>G	XP_011510231.1:p.Phe369Cys
XM_011511930.1:c.822T>G	XP_011510232.1:p.Phe274Leu
XM_011511929.2:c.1106T>G	XP_011510231.1:p.Phe369Cys
NM_025216.3:c.1202T>G MANE Select	NP_079492.2:p.Phe401Cys