Canonical Allele Identifier: CA2663173465
Gene: WNT10A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.218882207del , CM000664.2:g.218882207del GRCh38
NC_000002.11:g.219746929del , CM000664.1:g.219746929del GRCh37
NC_000002.10:g.219455173del NCBI36
NG_012179.1:g.6675del

Transcript Alleles

HGVS Amino-acid Change
ENST00000258411.8:c.160del MANE Select ENSP00000258411.3:p.Val54CysfsTer9
ENST00000258411.7:c.160del ENSP00000258411.3:p.Val54CysfsTer9
ENST00000458582.1:c.47del
NM_025216.2:c.160del NP_079492.2:p.Val54CysfsTer9
XM_011511928.1:c.109del XP_011510230.1:p.Val37CysfsTer9
XM_011511929.1:c.64del XP_011510231.1:p.Val22CysfsTer9
XM_011511930.1:c.160del XP_011510232.1:p.Val54CysfsTer9
XM_011511929.2:c.64del XP_011510231.1:p.Val22CysfsTer9
NM_025216.3:c.160del MANE Select NP_079492.2:p.Val54CysfsTer9