Canonical Allele Identifier: CA507318399
Community Standard Title: NM_001083961.2(WDR62):c.3936del (p.Val1313TrpfsTer12)
Gene: WDR62 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.36103764del , CM000681.2:g.36103764del GRCh38
NC_000019.9:g.36594666del , CM000681.1:g.36594666del GRCh37
NC_000019.8:g.41286506del NCBI36
NG_028101.1:g.53884del

Transcript Alleles

HGVS Amino-acid Change
NM_001083961.2:c.3936del MANE Select NP_001077430.1:p.Val1313TrpfsTer12
ENST00000401500.7:c.3936del MANE Select ENSP00000384792.1:p.Val1313TrpfsTer12
NM_001083961.1:c.3936del NP_001077430.1:p.Val1313TrpfsTer12
NM_173636.4:c.3921del NP_775907.4:p.Val1308TrpfsTer12
NM_173636.5:c.3921del NP_775907.4:p.Val1308TrpfsTer12
ENST00000270301.11:c.3921del ENSP00000270301.6:p.Val1308TrpfsTer12
ENST00000270301.12:c.3921del ENSP00000270301.6:p.Val1308TrpfsTer12
ENST00000401500.6:c.3936del ENSP00000384792.1:p.Val1313TrpfsTer12
ENST00000587391.5:c.*3796del ENSP00000465525.1:n.*3796del
ENST00000587391.6:c.*3796del ENSP00000465525.1:n.*3796del
ENST00000679357.1:c.2016del
ENST00000679598.1:c.701del
ENST00000679682.1:c.3921del ENSP00000506226.1:p.Val1308TrpfsTer12
ENST00000679714.1:c.3930del ENSP00000506627.1:p.Val1311TrpfsTer12
ENST00000679757.1:c.3585del ENSP00000505158.1:p.Val1196TrpfsTer12
ENST00000679858.1:c.*3318del ENSP00000505655.1:n.*3318del
ENST00000680211.1:c.537del ENSP00000506102.1:p.Val180TrpfsTer12
ENST00000680280.1:n.1439del
ENST00000680349.1:n.2585del
ENST00000680403.1:c.3921del ENSP00000505677.1:p.Val1308TrpfsTer12
ENST00000680564.1:c.3687del ENSP00000505582.1:p.Val1230TrpfsTer12
ENST00000680590.1:c.*2316del ENSP00000505350.1:n.*2316del
ENST00000680597.1:c.669del
ENST00000680739.1:c.951del
ENST00000680773.1:n.2437del
ENST00000680806.1:c.*3239del ENSP00000506418.1:n.*3239del
ENST00000680997.1:n.1868del
ENST00000681608.1:n.1781del
ENST00000681625.1:c.*1268del ENSP00000505555.1:n.*1268del
ENST00000681648.1:n.1451del
XM_005258809.2:c.3825del XP_005258866.1:p.Val1276TrpfsTer12
XM_011526837.1:c.3921del XP_011525139.1:p.Val1308TrpfsTer12
XM_011526838.1:c.3687del XP_011525140.1:p.Val1230TrpfsTer12
XM_011526839.1:c.3585del XP_011525141.1:p.Val1196TrpfsTer12
XM_011526840.1:c.2928del XP_011525142.1:p.Val977TrpfsTer12
XM_011526840.2:c.2928del XP_011525142.1:p.Val977TrpfsTer12
XM_011526841.1:c.2514del XP_011525143.1:p.Val839TrpfsTer12
XM_011526841.2:c.2514del XP_011525143.1:p.Val839TrpfsTer12
XM_011526842.1:c.2367del XP_011525144.1:p.Val790TrpfsTer12
XM_011526843.1:c.1683del XP_011525145.1:p.Val562TrpfsTer12
XM_011526844.1:c.1683del XP_011525146.1:p.Val562TrpfsTer12
XM_011526844.2:c.1683del XP_011525146.1:p.Val562TrpfsTer12
XM_017026665.1:c.3936del XP_016882154.1:p.Val1313TrpfsTer12