Canonical Allele Identifier: CA2956622777
Gene: WDR62 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.36104534_36104536del , CM000681.2:g.36104534_36104536del GRCh38
NC_000019.9:g.36595436_36595438del , CM000681.1:g.36595436_36595438del GRCh37
NC_000019.8:g.41287276_41287278del NCBI36
NG_028101.1:g.54654_54656del

Transcript Alleles

HGVS Amino-acid Change
ENST00000270301.12:c.4155_4157del ENSP00000270301.6:p.Gln1386del
ENST00000401500.7:c.4170_4172del MANE Select ENSP00000384792.1:p.Gln1391del
ENST00000587391.6:c.*4030_*4032del ENSP00000465525.1:n.*4030_*4032del
ENST00000679357.1:c.2250_2252del
ENST00000679598.1:c.919-4_919-2del
ENST00000679682.1:c.4155_4157del ENSP00000506226.1:p.Gln1386del
ENST00000679714.1:c.4164_4166del ENSP00000506627.1:p.Gln1389del
ENST00000679757.1:c.3819_3821del ENSP00000505158.1:p.Gln1274del
ENST00000679858.1:c.*3552_*3554del ENSP00000505655.1:n.*3552_*3554del
ENST00000680211.1:c.771_773del ENSP00000506102.1:p.Gln258del
ENST00000680280.1:n.1673_1675del
ENST00000680349.1:n.2819_2821del
ENST00000680403.1:c.4155_4157del ENSP00000505677.1:p.Gln1386del
ENST00000680564.1:c.3921_3923del ENSP00000505582.1:p.Gln1308del
ENST00000680590.1:c.*2550_*2552del ENSP00000505350.1:n.*2550_*2552del
ENST00000680597.1:c.903_905del
ENST00000680739.1:c.1185_1187del
ENST00000680773.1:n.2671_2673del
ENST00000680806.1:c.*3473_*3475del ENSP00000506418.1:n.*3473_*3475del
ENST00000680997.1:n.2102_2104del
ENST00000681608.1:n.2015_2017del
ENST00000681625.1:c.*1502_*1504del ENSP00000505555.1:n.*1502_*1504del
ENST00000681648.1:n.2221_2223del
ENST00000270301.11:c.4155_4157del ENSP00000270301.6:p.Gln1386del
ENST00000401500.6:c.4170_4172del ENSP00000384792.1:p.Gln1391del
ENST00000587391.5:c.*4030_*4032del ENSP00000465525.1:n.*4030_*4032del
NM_001083961.1:c.4170_4172del NP_001077430.1:p.Gln1391del
NM_173636.4:c.4155_4157del NP_775907.4:p.Gln1386del
XM_005258809.2:c.4059_4061del XP_005258866.1:p.Gln1354del
XM_011526837.1:c.4155_4157del XP_011525139.1:p.Gln1386del
XM_011526838.1:c.3921_3923del XP_011525140.1:p.Gln1308del
XM_011526839.1:c.3819_3821del XP_011525141.1:p.Gln1274del
XM_011526840.1:c.3162_3164del XP_011525142.1:p.Gln1055del
XM_011526841.1:c.2748_2750del XP_011525143.1:p.Gln917del
XM_011526842.1:c.2601_2603del XP_011525144.1:p.Gln868del
XM_011526843.1:c.1917_1919del XP_011525145.1:p.Gln640del
XM_011526844.1:c.1917_1919del XP_011525146.1:p.Gln640del
XM_011526840.2:c.3162_3164del XP_011525142.1:p.Gln1055del
XM_011526841.2:c.2748_2750del XP_011525143.1:p.Gln917del
XM_011526844.2:c.1917_1919del XP_011525146.1:p.Gln640del
XM_017026665.1:c.4170_4172del XP_016882154.1:p.Gln1391del
NM_001083961.2:c.4170_4172del MANE Select NP_001077430.1:p.Gln1391del
NM_173636.5:c.4155_4157del NP_775907.4:p.Gln1386del