Canonical Allele Identifier: CA2113841
Gene: WNT10A HGNC NCBI

Linked Data

ClinVar Variation Id: 2947030
ClinVar RCV Id: RCV003801220
dbSNP Id: rs749297006
ExAC: 2:219746915 TC / T
gnomAD v2: 2-219746915-TC-T
gnomAD v4: 2-218882193-TC-T
COSMIC: COSM4439893
MyVariant Identifiers: chr2:g.219746916del (hg19) chr2:g.218882194del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.218882199del , CM000664.2:g.218882199del GRCh38
NC_000002.11:g.219746921del , CM000664.1:g.219746921del GRCh37
NC_000002.10:g.219455165del NCBI36
NG_012179.1:g.6667del

Transcript Alleles

HGVS Amino-acid Change
ENST00000258411.8:c.152del MANE Select ENSP00000258411.3:p.Pro51ArgfsTer12
ENST00000258411.7:c.152del ENSP00000258411.3:p.Pro51ArgfsTer12
ENST00000458582.1:c.39del
NM_025216.2:c.152del NP_079492.2:p.Pro51ArgfsTer12
XM_011511928.1:c.101del XP_011510230.1:p.Pro34ArgfsTer12
XM_011511929.1:c.56del XP_011510231.1:p.Pro19ArgfsTer12
XM_011511930.1:c.152del XP_011510232.1:p.Pro51ArgfsTer12
XM_011511929.2:c.56del XP_011510231.1:p.Pro19ArgfsTer12
NM_025216.3:c.152del MANE Select NP_079492.2:p.Pro51ArgfsTer12
Search 100 bp 5'
Search 100 bp 3'