Canonical Allele Identifier: CA251360
Gene: WDR62 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.36104569_36104572del , CM000681.2:g.36104569_36104572del GRCh38
NC_000019.9:g.36595471_36595474del , CM000681.1:g.36595471_36595474del GRCh37
NC_000019.8:g.41287311_41287314del NCBI36
NG_028101.1:g.54689_54692del

Transcript Alleles

HGVS Amino-acid Change
ENST00000270301.12:c.4190_4193del ENSP00000270301.6:p.Val1397GlyfsTer12
ENST00000401500.7:c.4205_4208del MANE Select ENSP00000384792.1:p.Val1402GlyfsTer12
ENST00000587391.6:c.*4065_*4068del ENSP00000465525.1:n.*4065_*4068del
ENST00000679357.1:c.2285_2288del
ENST00000679598.1:c.950_953del
ENST00000679682.1:c.4190_4193del ENSP00000506226.1:p.Val1397GlyfsTer12
ENST00000679714.1:c.4199_4202del ENSP00000506627.1:p.Val1400GlyfsTer12
ENST00000679757.1:c.3854_3857del ENSP00000505158.1:p.Val1285GlyfsTer12
ENST00000679858.1:c.*3587_*3590del ENSP00000505655.1:n.*3587_*3590del
ENST00000680211.1:c.806_809del ENSP00000506102.1:p.Val269GlyfsTer12
ENST00000680280.1:n.1708_1711del
ENST00000680349.1:n.2854_2857del
ENST00000680403.1:c.4190_4193del ENSP00000505677.1:p.Val1397GlyfsTer12
ENST00000680564.1:c.3956_3959del ENSP00000505582.1:p.Val1319GlyfsTer12
ENST00000680590.1:c.*2585_*2588del ENSP00000505350.1:n.*2585_*2588del
ENST00000680597.1:c.938_941del
ENST00000680739.1:c.1220_1223del
ENST00000680773.1:n.2706_2709del
ENST00000680806.1:c.*3508_*3511del ENSP00000506418.1:n.*3508_*3511del
ENST00000680997.1:n.2137_2140del
ENST00000681608.1:n.2050_2053del
ENST00000681625.1:c.*1537_*1540del ENSP00000505555.1:n.*1537_*1540del
ENST00000681648.1:n.2256_2259del
ENST00000270301.11:c.4190_4193del ENSP00000270301.6:p.Val1397GlyfsTer12
ENST00000401500.6:c.4205_4208del ENSP00000384792.1:p.Val1402GlyfsTer12
ENST00000587391.5:c.*4065_*4068del ENSP00000465525.1:n.*4065_*4068del
NM_001083961.1:c.4205_4208del NP_001077430.1:p.Val1402GlyfsTer12
NM_173636.4:c.4190_4193del NP_775907.4:p.Val1397GlyfsTer12
XM_005258809.2:c.4094_4097del XP_005258866.1:p.Val1365GlyfsTer12
XM_011526837.1:c.4190_4193del XP_011525139.1:p.Val1397GlyfsTer12
XM_011526838.1:c.3956_3959del XP_011525140.1:p.Val1319GlyfsTer12
XM_011526839.1:c.3854_3857del XP_011525141.1:p.Val1285GlyfsTer12
XM_011526840.1:c.3197_3200del XP_011525142.1:p.Val1066GlyfsTer12
XM_011526841.1:c.2783_2786del XP_011525143.1:p.Val928GlyfsTer12
XM_011526842.1:c.2636_2639del XP_011525144.1:p.Val879GlyfsTer12
XM_011526843.1:c.1952_1955del XP_011525145.1:p.Val651GlyfsTer12
XM_011526844.1:c.1952_1955del XP_011525146.1:p.Val651GlyfsTer12
XM_011526840.2:c.3197_3200del XP_011525142.1:p.Val1066GlyfsTer12
XM_011526841.2:c.2783_2786del XP_011525143.1:p.Val928GlyfsTer12
XM_011526844.2:c.1952_1955del XP_011525146.1:p.Val651GlyfsTer12
XM_017026665.1:c.4205_4208del XP_016882154.1:p.Val1402GlyfsTer12
NM_001083961.2:c.4205_4208del MANE Select NP_001077430.1:p.Val1402GlyfsTer12
NM_173636.5:c.4190_4193del NP_775907.4:p.Val1397GlyfsTer12