Canonical Allele Identifier: CA2333970947
Gene: WDR62 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.36102117C= , CM000681.2:g.36102117C= GRCh38
NC_000019.9:g.36593019C= , CM000681.1:g.36593019C= GRCh37
NC_000019.8:g.41284859C= NCBI36
NG_028101.1:g.52237C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000270301.12:c.3186C= ENSP00000270301.6:p.His1062=
ENST00000401500.7:c.3186C= MANE Select ENSP00000384792.1:p.His1062=
ENST00000587391.6:c.*2461C= ENSP00000465525.1:n.*2461C=
ENST00000679357.1:c.976C=
ENST00000679422.1:c.865C=
ENST00000679682.1:c.3171C= ENSP00000506226.1:p.His1057=
ENST00000679714.1:c.3180C= ENSP00000506627.1:p.His1060=
ENST00000679757.1:c.2835C= ENSP00000505158.1:p.His945=
ENST00000679858.1:c.*2568C= ENSP00000505655.1:n.*2568C=
ENST00000680211.1:c.-214C= ENSP00000506102.1:n.-214C=
ENST00000680349.1:n.1169C=
ENST00000680403.1:c.3186C= ENSP00000505677.1:p.His1062=
ENST00000680564.1:c.2972-620C= ENSP00000505582.1:n.2972-620C=
ENST00000680590.1:c.*1581C= ENSP00000505350.1:n.*1581C=
ENST00000680739.1:c.104C=
ENST00000680773.1:n.1102C=
ENST00000680806.1:c.*1904C= ENSP00000506418.1:n.*1904C=
ENST00000680997.1:n.533C=
ENST00000681088.1:c.848C=
ENST00000681608.1:n.134C=
ENST00000681625.1:c.*518C= ENSP00000505555.1:n.*518C=
ENST00000270301.11:c.3186C= ENSP00000270301.6:p.His1062=
ENST00000401500.6:c.3186C= ENSP00000384792.1:p.His1062=
ENST00000587391.5:c.*2461C= ENSP00000465525.1:n.*2461C=
NM_001083961.1:c.3186C= NP_001077430.1:p.His1062=
NM_173636.4:c.3186C= NP_775907.4:p.His1062=
XM_005258809.2:c.3075C= XP_005258866.1:p.His1025=
XM_011526837.1:c.3171C= XP_011525139.1:p.His1057=
XM_011526838.1:c.2972-620C= XP_011525140.1:n.2972-620C=
XM_011526839.1:c.2835C= XP_011525141.1:p.His945=
XM_011526840.1:c.2178C= XP_011525142.1:p.His726=
XM_011526841.1:c.1764C= XP_011525143.1:p.His588=
XM_011526842.1:c.1617C= XP_011525144.1:p.His539=
XM_011526843.1:c.933C= XP_011525145.1:p.His311=
XM_011526844.1:c.933C= XP_011525146.1:p.His311=
XM_011526840.2:c.2178C= XP_011525142.1:p.His726=
XM_011526841.2:c.1764C= XP_011525143.1:p.His588=
XM_011526844.2:c.933C= XP_011525146.1:p.His311=
XM_017026665.1:c.3186C= XP_016882154.1:p.His1062=
NM_001083961.2:c.3186C= MANE Select NP_001077430.1:p.His1062=
NM_173636.5:c.3186C= NP_775907.4:p.His1062=