Canonical Allele Identifier: CA2333970943
Gene: WDR62 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.36102112C= , CM000681.2:g.36102112C= GRCh38
NC_000019.9:g.36593014C= , CM000681.1:g.36593014C= GRCh37
NC_000019.8:g.41284854C= NCBI36
NG_028101.1:g.52232C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000270301.12:c.3181C= ENSP00000270301.6:p.Arg1061=
ENST00000401500.7:c.3181C= MANE Select ENSP00000384792.1:p.Arg1061=
ENST00000587391.6:c.*2456C= ENSP00000465525.1:n.*2456C=
ENST00000679357.1:c.971C=
ENST00000679422.1:c.860C=
ENST00000679682.1:c.3166C= ENSP00000506226.1:p.Arg1056=
ENST00000679714.1:c.3175C= ENSP00000506627.1:p.Arg1059=
ENST00000679757.1:c.2830C= ENSP00000505158.1:p.Arg944=
ENST00000679858.1:c.*2563C= ENSP00000505655.1:n.*2563C=
ENST00000680211.1:c.-219C= ENSP00000506102.1:n.-219C=
ENST00000680349.1:n.1164C=
ENST00000680403.1:c.3181C= ENSP00000505677.1:p.Arg1061=
ENST00000680564.1:c.2972-625C= ENSP00000505582.1:n.2972-625C=
ENST00000680590.1:c.*1576C= ENSP00000505350.1:n.*1576C=
ENST00000680739.1:c.99C=
ENST00000680773.1:n.1097C=
ENST00000680806.1:c.*1899C= ENSP00000506418.1:n.*1899C=
ENST00000680997.1:n.528C=
ENST00000681088.1:c.843C=
ENST00000681608.1:n.129C=
ENST00000681625.1:c.*513C= ENSP00000505555.1:n.*513C=
ENST00000270301.11:c.3181C= ENSP00000270301.6:p.Arg1061=
ENST00000401500.6:c.3181C= ENSP00000384792.1:p.Arg1061=
ENST00000587391.5:c.*2456C= ENSP00000465525.1:n.*2456C=
NM_001083961.1:c.3181C= NP_001077430.1:p.Arg1061=
NM_173636.4:c.3181C= NP_775907.4:p.Arg1061=
XM_005258809.2:c.3070C= XP_005258866.1:p.Arg1024=
XM_011526837.1:c.3166C= XP_011525139.1:p.Arg1056=
XM_011526838.1:c.2972-625C= XP_011525140.1:n.2972-625C=
XM_011526839.1:c.2830C= XP_011525141.1:p.Arg944=
XM_011526840.1:c.2173C= XP_011525142.1:p.Arg725=
XM_011526841.1:c.1759C= XP_011525143.1:p.Arg587=
XM_011526842.1:c.1612C= XP_011525144.1:p.Arg538=
XM_011526843.1:c.928C= XP_011525145.1:p.Arg310=
XM_011526844.1:c.928C= XP_011525146.1:p.Arg310=
XM_011526840.2:c.2173C= XP_011525142.1:p.Arg725=
XM_011526841.2:c.1759C= XP_011525143.1:p.Arg587=
XM_011526844.2:c.928C= XP_011525146.1:p.Arg310=
XM_017026665.1:c.3181C= XP_016882154.1:p.Arg1061=
NM_001083961.2:c.3181C= MANE Select NP_001077430.1:p.Arg1061=
NM_173636.5:c.3181C= NP_775907.4:p.Arg1061=