Canonical Allele Identifier: CA251365
Gene: WDR62 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.36103667_36103683del , CM000681.2:g.36103667_36103683del GRCh38
NC_000019.9:g.36594569_36594585del , CM000681.1:g.36594569_36594585del GRCh37
NC_000019.8:g.41286409_41286425del NCBI36
NG_028101.1:g.53787_53803del

Transcript Alleles

HGVS Amino-acid Change
ENST00000270301.12:c.3824_3840del ENSP00000270301.6:p.Gly1275AlafsTer21
ENST00000401500.7:c.3839_3855del MANE Select ENSP00000384792.1:p.Gly1280AlafsTer21
ENST00000587391.6:c.*3699_*3715del ENSP00000465525.1:n.*3699_*3715del
ENST00000679357.1:c.1919_1935del
ENST00000679598.1:c.604_620del
ENST00000679682.1:c.3824_3840del ENSP00000506226.1:p.Gly1275AlafsTer21
ENST00000679714.1:c.3833_3849del ENSP00000506627.1:p.Gly1278AlafsTer21
ENST00000679757.1:c.3488_3504del ENSP00000505158.1:p.Gly1163AlafsTer21
ENST00000679858.1:c.*3221_*3237del ENSP00000505655.1:n.*3221_*3237del
ENST00000680211.1:c.440_456del ENSP00000506102.1:p.Gly147AlafsTer21
ENST00000680280.1:n.1342_1358del
ENST00000680349.1:n.2488_2504del
ENST00000680403.1:c.3824_3840del ENSP00000505677.1:p.Gly1275AlafsTer21
ENST00000680564.1:c.3590_3606del ENSP00000505582.1:p.Gly1197AlafsTer21
ENST00000680590.1:c.*2219_*2235del ENSP00000505350.1:n.*2219_*2235del
ENST00000680597.1:c.572_588del
ENST00000680739.1:c.854_870del
ENST00000680773.1:n.2340_2356del
ENST00000680806.1:c.*3142_*3158del ENSP00000506418.1:n.*3142_*3158del
ENST00000680997.1:n.1771_1787del
ENST00000681608.1:n.1684_1700del
ENST00000681625.1:c.*1171_*1187del ENSP00000505555.1:n.*1171_*1187del
ENST00000681648.1:n.1354_1370del
ENST00000270301.11:c.3824_3840del ENSP00000270301.6:p.Gly1275AlafsTer21
ENST00000401500.6:c.3839_3855del ENSP00000384792.1:p.Gly1280AlafsTer21
ENST00000587391.5:c.*3699_*3715del ENSP00000465525.1:n.*3699_*3715del
NM_001083961.1:c.3839_3855del NP_001077430.1:p.Gly1280AlafsTer21
NM_173636.4:c.3824_3840del NP_775907.4:p.Gly1275AlafsTer21
XM_005258809.2:c.3728_3744del XP_005258866.1:p.Gly1243AlafsTer21
XM_011526837.1:c.3824_3840del XP_011525139.1:p.Gly1275AlafsTer21
XM_011526838.1:c.3590_3606del XP_011525140.1:p.Gly1197AlafsTer21
XM_011526839.1:c.3488_3504del XP_011525141.1:p.Gly1163AlafsTer21
XM_011526840.1:c.2831_2847del XP_011525142.1:p.Gly944AlafsTer21
XM_011526841.1:c.2417_2433del XP_011525143.1:p.Gly806AlafsTer21
XM_011526842.1:c.2270_2286del XP_011525144.1:p.Gly757AlafsTer21
XM_011526843.1:c.1586_1602del XP_011525145.1:p.Gly529AlafsTer21
XM_011526844.1:c.1586_1602del XP_011525146.1:p.Gly529AlafsTer21
XM_011526840.2:c.2831_2847del XP_011525142.1:p.Gly944AlafsTer21
XM_011526841.2:c.2417_2433del XP_011525143.1:p.Gly806AlafsTer21
XM_011526844.2:c.1586_1602del XP_011525146.1:p.Gly529AlafsTer21
XM_017026665.1:c.3839_3855del XP_016882154.1:p.Gly1280AlafsTer21
NM_001083961.2:c.3839_3855del MANE Select NP_001077430.1:p.Gly1280AlafsTer21
NM_173636.5:c.3824_3840del NP_775907.4:p.Gly1275AlafsTer21