Canonical Allele Identifier: CA2843142785
Gene: WNT10A HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.218893254del , CM000664.2:g.218893254del GRCh38
NC_000002.11:g.219757976del , CM000664.1:g.219757976del GRCh37
NC_000002.10:g.219466220del NCBI36
NG_012179.1:g.17722del

Transcript Alleles

HGVS Amino-acid Change
ENST00000258411.8:c.1237del MANE Select ENSP00000258411.3:p.Val413SerfsTer25
ENST00000258411.7:c.1237del ENSP00000258411.3:p.Val413SerfsTer25
ENST00000489887.1:n.34del
NM_025216.2:c.1237del NP_079492.2:p.Val413SerfsTer25
XM_011511928.1:c.1186del XP_011510230.1:p.Val396SerfsTer25
XM_011511929.1:c.1141del XP_011510231.1:p.Val381SerfsTer25
XM_011511930.1:c.857del XP_011510232.1:p.Gly286ValfsTer6
XM_011511929.2:c.1141del XP_011510231.1:p.Val381SerfsTer25
NM_025216.3:c.1237del MANE Select NP_079492.2:p.Val413SerfsTer25
Search 100 bp 5'
Search 100 bp 3'