Canonical Allele Identifier: CA2113989

Gene: WNT10A

Linked Data

• ClinVar Variation Id: 702777
• ClinVar RCV Id: RCV000872013 ; RCV001271494
• dbSNP Id: rs765046353
• ExAC: 2:219754989 C / T
• gnomAD v2: 2-219754989-C-T
• gnomAD v3: 2-218890267-C-T
• gnomAD v4: 2-218890267-C-T
• COSMIC: COSM3713615
• MyVariant Identifiers: chr2:g.219754989C>T (hg19) ; chr2:g.218890267C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218890267C>T , CM000664.2:g.218890267C>T	GRCh38
NC_000002.11:g.219754989C>T , CM000664.1:g.219754989C>T	GRCh37
NC_000002.10:g.219463233C>T	NCBI36
NG_012179.1:g.14735C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000258411.8:c.660C>T MANE Select	ENSP00000258411.3:p.Phe220=
ENST00000258411.7:c.660C>T	ENSP00000258411.3:p.Phe220=
ENST00000458582.1:c.264-2507C>T
NM_025216.2:c.660C>T	NP_079492.2:p.Phe220=
XM_011511928.1:c.609C>T	XP_011510230.1:p.Phe203=
XM_011511929.1:c.564C>T	XP_011510231.1:p.Phe188=
XM_011511930.1:c.377-2507C>T	XP_011510232.1:n.377-2507C>T
XM_011511929.2:c.564C>T	XP_011510231.1:p.Phe188=
NM_025216.3:c.660C>T MANE Select	NP_079492.2:p.Phe220=