Canonical Allele Identifier: CA2333972222
Gene: WDR62 HGNC NCBI

Linked Data

dbSNP Id: rs1973625591

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.36104627_36104628insGTGGTCTG , CM000681.2:g.36104627_36104628insGTGGTCTG GRCh38
NC_000019.9:g.36595529_36595530insGTGGTCTG , CM000681.1:g.36595529_36595530insGTGGTCTG GRCh37
NC_000019.8:g.41287369_41287370insGTGGTCTG NCBI36
NG_028101.1:g.54747_54748insGTGGTCTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000270301.12:c.4248_4249insGTGGTCTG ENSP00000270301.6:p.His1417ValfsTer?
ENST00000401500.7:c.4263_4264insGTGGTCTG MANE Select ENSP00000384792.1:p.His1422ValfsTer?
ENST00000587391.6:c.*4123_*4124insGTGGTCTG ENSP00000465525.1:n.*4123_*4124insGTGGTCTG
ENST00000679357.1:c.2343_2344insGTGGTCTG
ENST00000679598.1:c.1008_1009insGTGGTCTG
ENST00000679682.1:c.4248_4249insGTGGTCTG ENSP00000506226.1:p.His1417ValfsTer?
ENST00000679714.1:c.4257_4258insGTGGTCTG ENSP00000506627.1:p.His1420ValfsTer?
ENST00000679757.1:c.3912_3913insGTGGTCTG ENSP00000505158.1:p.His1305ValfsTer?
ENST00000679858.1:c.*3645_*3646insGTGGTCTG ENSP00000505655.1:n.*3645_*3646insGTGGTCTG
ENST00000680211.1:c.864_865insGTGGTCTG ENSP00000506102.1:p.His289ValfsTer?
ENST00000680280.1:n.1766_1767insGTGGTCTG
ENST00000680349.1:n.2912_2913insGTGGTCTG
ENST00000680403.1:c.4248_4249insGTGGTCTG ENSP00000505677.1:p.His1417ValfsTer20
ENST00000680564.1:c.4014_4015insGTGGTCTG ENSP00000505582.1:p.His1339ValfsTer?
ENST00000680590.1:c.*2643_*2644insGTGGTCTG ENSP00000505350.1:n.*2643_*2644insGTGGTCTG
ENST00000680597.1:c.996_997insGTGGTCTG
ENST00000680739.1:c.1278_1279insGTGGTCTG
ENST00000680773.1:n.2764_2765insGTGGTCTG
ENST00000680806.1:c.*3566_*3567insGTGGTCTG ENSP00000506418.1:n.*3566_*3567insGTGGTCTG
ENST00000680997.1:n.2195_2196insGTGGTCTG
ENST00000681608.1:n.2108_2109insGTGGTCTG
ENST00000681625.1:c.*1595_*1596insGTGGTCTG ENSP00000505555.1:n.*1595_*1596insGTGGTCTG
ENST00000681648.1:n.2314_2315insGTGGTCTG
ENST00000270301.11:c.4248_4249insGTGGTCTG ENSP00000270301.6:p.His1417ValfsTer?
ENST00000401500.6:c.4263_4264insGTGGTCTG ENSP00000384792.1:p.His1422ValfsTer?
ENST00000587391.5:c.*4123_*4124insGTGGTCTG ENSP00000465525.1:n.*4123_*4124insGTGGTCTG
NM_001083961.1:c.4263_4264insGTGGTCTG NP_001077430.1:p.His1422ValfsTer?
NM_173636.4:c.4248_4249insGTGGTCTG NP_775907.4:p.His1417ValfsTer?
XM_005258809.2:c.4152_4153insGTGGTCTG XP_005258866.1:p.His1385ValfsTer?
XM_011526837.1:c.4248_4249insGTGGTCTG XP_011525139.1:p.His1417ValfsTer?
XM_011526838.1:c.4014_4015insGTGGTCTG XP_011525140.1:p.His1339ValfsTer?
XM_011526839.1:c.3912_3913insGTGGTCTG XP_011525141.1:p.His1305ValfsTer?
XM_011526840.1:c.3255_3256insGTGGTCTG XP_011525142.1:p.His1086ValfsTer?
XM_011526841.1:c.2841_2842insGTGGTCTG XP_011525143.1:p.His948ValfsTer?
XM_011526842.1:c.2694_2695insGTGGTCTG XP_011525144.1:p.His899ValfsTer?
XM_011526843.1:c.2010_2011insGTGGTCTG XP_011525145.1:p.His671ValfsTer?
XM_011526844.1:c.2010_2011insGTGGTCTG XP_011525146.1:p.His671ValfsTer?
XM_011526840.2:c.3255_3256insGTGGTCTG XP_011525142.1:p.His1086ValfsTer?
XM_011526841.2:c.2841_2842insGTGGTCTG XP_011525143.1:p.His948ValfsTer?
XM_011526844.2:c.2010_2011insGTGGTCTG XP_011525146.1:p.His671ValfsTer?
XM_017026665.1:c.4263_4264insGTGGTCTG XP_016882154.1:p.His1422ValfsTer?
NM_001083961.2:c.4263_4264insGTGGTCTG MANE Select NP_001077430.1:p.His1422ValfsTer?
NM_173636.5:c.4248_4249insGTGGTCTG NP_775907.4:p.His1417ValfsTer?