Canonical Allele Identifier: CA2113858
Gene: WNT10A HGNC NCBI

Linked Data

ClinVar Variation Id: 334394
ClinVar RCV Id: RCV000308592 RCV000401069 RCV000639740 RCV001545215 RCV000358786 RCV004530357
dbSNP Id: rs146460077
ExAC: 2:219746977 C / T
gnomAD v2: 2-219746977-C-T
gnomAD v3: 2-218882255-C-T
gnomAD v4: 2-218882255-C-T
COSMIC: COSM1565077
MyVariant Identifiers: chr2:g.219746977C>T (hg19) chr2:g.218882255C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.218882255C>T , CM000664.2:g.218882255C>T GRCh38
NC_000002.11:g.219746977C>T , CM000664.1:g.219746977C>T GRCh37
NC_000002.10:g.219455221C>T NCBI36
NG_012179.1:g.6723C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000258411.8:c.208C>T MANE Select ENSP00000258411.3:p.Arg70Trp
ENST00000258411.7:c.208C>T ENSP00000258411.3:p.Arg70Trp
ENST00000458582.1:c.95C>T
NM_025216.2:c.208C>T NP_079492.2:p.Arg70Trp
XM_011511928.1:c.157C>T XP_011510230.1:p.Arg53Trp
XM_011511929.1:c.112C>T XP_011510231.1:p.Arg38Trp
XM_011511930.1:c.208C>T XP_011510232.1:p.Arg70Trp
XM_011511929.2:c.112C>T XP_011510231.1:p.Arg38Trp
NM_025216.3:c.208C>T MANE Select NP_079492.2:p.Arg70Trp
Search 100 bp 5'
Search 100 bp 3'