Canonical Allele Identifier: CA116865

Gene: WNT10A

Linked Data

• ClinVar Variation Id: 4461
• ClinVar RCV Id: RCV000004715 ; RCV000004716 ; RCV000030650 ; RCV000190800 ; RCV000255732 ; RCV000536747 ; RCV000477935 ; RCV000779308 ; RCV001729335 ; RCV002247247
• dbSNP Id: rs121908119
• ExAC: 2:219747090 C / A
• gnomAD v2: 2-219747090-C-A
• gnomAD v3: 2-218882368-C-A
• gnomAD v4: 2-218882368-C-A
• MyVariant Identifiers: chr2:g.219747090C>A (hg19) ; chr2:g.218882368C>A (hg38)
• PubMed: PMID:17847007 ; PMID:19559398 ; PMID:22581971 ; PMID:23167694 ; PMID:23401279 ; PMID:24043634 ; PMID:24398796 ; PMID:24700731 ; PMID:24702986 ; PMID:24902757 ; PMID:25356970 ; PMID:25629078 ; PMID:28105635

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218882368C>A , CM000664.2:g.218882368C>A	GRCh38
NC_000002.11:g.219747090C>A , CM000664.1:g.219747090C>A	GRCh37
NC_000002.10:g.219455334C>A	NCBI36
NG_012179.1:g.6836C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258411.8:c.321C>A MANE Select	ENSP00000258411.3:p.Cys107Ter
ENST00000258411.7:c.321C>A	ENSP00000258411.3:p.Cys107Ter
ENST00000458582.1:c.208C>A
NM_025216.2:c.321C>A	NP_079492.2:p.Cys107Ter
XM_011511928.1:c.270C>A	XP_011510230.1:p.Cys90Ter
XM_011511929.1:c.225C>A	XP_011510231.1:p.Cys75Ter
XM_011511930.1:c.321C>A	XP_011510232.1:p.Cys107Ter
XM_011511929.2:c.225C>A	XP_011510231.1:p.Cys75Ter
NM_025216.3:c.321C>A MANE Select	NP_079492.2:p.Cys107Ter