Canonical Allele Identifier: CA350592711

Gene: WNT10A

Linked Data

• dbSNP Id: rs1944679304
• gnomAD v3: 2-218893238-C-A
• gnomAD v4: 2-218893238-C-A
• MyVariant Identifiers: chr2:g.219757960C>A (hg19) ; chr2:g.218893238C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218893238C>A , CM000664.2:g.218893238C>A	GRCh38
NC_000002.11:g.219757960C>A , CM000664.1:g.219757960C>A	GRCh37
NC_000002.10:g.219466204C>A	NCBI36
NG_012179.1:g.17706C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258411.8:c.1221C>A MANE Select	ENSP00000258411.3:p.Cys407Ter
ENST00000258411.7:c.1221C>A	ENSP00000258411.3:p.Cys407Ter
ENST00000489887.1:n.18C>A
NM_025216.2:c.1221C>A	NP_079492.2:p.Cys407Ter
XM_011511928.1:c.1170C>A	XP_011510230.1:p.Cys390Ter
XM_011511929.1:c.1125C>A	XP_011510231.1:p.Cys375Ter
XM_011511930.1:c.841C>A	XP_011510232.1:p.Pro281Thr
XM_011511929.2:c.1125C>A	XP_011510231.1:p.Cys375Ter
NM_025216.3:c.1221C>A MANE Select	NP_079492.2:p.Cys407Ter