Canonical Allele Identifier: CA116869

Gene: WNT10A

Linked Data

• ClinVar Variation Id: 4464
• ClinVar RCV Id: RCV003764526
• dbSNP Id: rs121908122
• MyVariant Identifiers: chr2:g.219757867C>A (hg19) ; chr2:g.218893145C>A (hg38)
• PubMed: PMID:19559398

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218893145C>A , CM000664.2:g.218893145C>A	GRCh38
NC_000002.11:g.219757867C>A , CM000664.1:g.219757867C>A	GRCh37
NC_000002.10:g.219466111C>A	NCBI36
NG_012179.1:g.17613C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000258411.8:c.1128C>A MANE Select	ENSP00000258411.3:p.Cys376Ter
ENST00000258411.7:c.1128C>A	ENSP00000258411.3:p.Cys376Ter
ENST00000458582.1:c.635C>A
NM_025216.2:c.1128C>A	NP_079492.2:p.Cys376Ter
XM_011511928.1:c.1077C>A	XP_011510230.1:p.Cys359Ter
XM_011511929.1:c.1032C>A	XP_011510231.1:p.Cys344Ter
XM_011511930.1:c.748C>A	XP_011510232.1:p.Leu250Met
XM_011511929.2:c.1032C>A	XP_011510231.1:p.Cys344Ter
NM_025216.3:c.1128C>A MANE Select	NP_079492.2:p.Cys376Ter