Canonical Allele Identifier: CA764938277
Gene: WNT10A HGNC NCBI

Linked Data

dbSNP Id: rs1175827745
gnomAD v3: 2-218881698-CTT-C
gnomAD v4: 2-218881698-CTT-C
MyVariant Identifiers: chr2:g.219746421_219746422del (hg19) chr2:g.218881699_218881700del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.218881700_218881701del , CM000664.2:g.218881700_218881701del GRCh38
NC_000002.11:g.219746422_219746423del , CM000664.1:g.219746422_219746423del GRCh37
NC_000002.10:g.219454666_219454667del NCBI36
NG_012179.1:g.6168_6169del

Transcript Alleles

HGVS Amino-acid Change
ENST00000258411.8:c.114-461_114-460del MANE Select ENSP00000258411.3:n.114-461_114-460del
ENST00000258411.7:c.114-461_114-460del ENSP00000258411.3:n.114-461_114-460del
NM_025216.2:c.114-461_114-460del NP_079492.2:n.114-461_114-460del
XM_011511928.1:c.62+233_62+234del XP_011510230.1:n.62+233_62+234del
XM_011511929.1:c.18-461_18-460del XP_011510231.1:n.18-461_18-460del
XM_011511930.1:c.114-461_114-460del XP_011510232.1:n.114-461_114-460del
XM_011511929.2:c.18-461_18-460del XP_011510231.1:n.18-461_18-460del
NM_025216.3:c.114-461_114-460del MANE Select NP_079492.2:n.114-461_114-460del
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