Canonical Allele Identifier: CA764938631
Gene: WNT10A HGNC NCBI

Linked Data

dbSNP Id: rs1239958962
MyVariant Identifiers: chr2:g.219746964del (hg19) chr2:g.218882242del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.218882242del , CM000664.2:g.218882242del GRCh38
NC_000002.11:g.219746964del , CM000664.1:g.219746964del GRCh37
NC_000002.10:g.219455208del NCBI36
NG_012179.1:g.6710del

Transcript Alleles

HGVS Amino-acid Change
ENST00000258411.8:c.195del MANE Select ENSP00000258411.3:p.Gly66AlafsTer2
ENST00000258411.7:c.195del ENSP00000258411.3:p.Gly66AlafsTer2
ENST00000458582.1:c.82del
NM_025216.2:c.195del NP_079492.2:p.Gly66AlafsTer2
XM_011511928.1:c.144del XP_011510230.1:p.Gly49AlafsTer2
XM_011511929.1:c.99del XP_011510231.1:p.Gly34AlafsTer2
XM_011511930.1:c.195del XP_011510232.1:p.Gly66AlafsTer2
XM_011511929.2:c.99del XP_011510231.1:p.Gly34AlafsTer2
NM_025216.3:c.195del MANE Select NP_079492.2:p.Gly66AlafsTer2
Search 100 bp 5'
Search 100 bp 3'