Canonical Allele Identifier: CA1328965692
Gene: WNT10A HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.218893275_218893276delinsGC , CM000664.2:g.218893275_218893276delinsGC GRCh38
NC_000002.11:g.219757997_219757998delinsGC , CM000664.1:g.219757997_219757998delinsGC GRCh37
NC_000002.10:g.219466241_219466242delinsGC NCBI36
NG_012179.1:g.17743_17744delinsGC

Transcript Alleles

HGVS Amino-acid change
ENST00000258411.8:c.*4_*5delinsGC MANE Select ENSP00000258411.3:n.*4_*5delinsGC
ENST00000258411.7:c.*4_*5delinsGC ENSP00000258411.3:n.*4_*5delinsGC
ENST00000489887.1:n.47+8_47+9delinsGC
NM_025216.2:c.*4_*5delinsGC NP_079492.2:n.*4_*5delinsGC
XM_011511928.1:c.*4_*5delinsGC XP_011510230.1:n.*4_*5delinsGC
XM_011511929.1:c.*4_*5delinsGC XP_011510231.1:n.*4_*5delinsGC
XM_011511930.1:c.878_879delinsGC XP_011510232.1:p.Gly293=
XM_011511929.2:c.*4_*5delinsGC XP_011510231.1:n.*4_*5delinsGC
NM_025216.3:c.*4_*5delinsGC MANE Select NP_079492.2:n.*4_*5delinsGC
Search 100 bp 5'
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