Canonical Allele Identifier: CA2333972200
Gene: WDR62 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.36104582C= , CM000681.2:g.36104582C= GRCh38
NC_000019.9:g.36595484C= , CM000681.1:g.36595484C= GRCh37
NC_000019.8:g.41287324C= NCBI36
NG_028101.1:g.54702C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000270301.12:c.4203C= ENSP00000270301.6:p.Ala1401=
ENST00000401500.7:c.4218C= MANE Select ENSP00000384792.1:p.Ala1406=
ENST00000587391.6:c.*4078C= ENSP00000465525.1:n.*4078C=
ENST00000679357.1:c.2298C=
ENST00000679598.1:c.963C=
ENST00000679682.1:c.4203C= ENSP00000506226.1:p.Ala1401=
ENST00000679714.1:c.4212C= ENSP00000506627.1:p.Ala1404=
ENST00000679757.1:c.3867C= ENSP00000505158.1:p.Ala1289=
ENST00000679858.1:c.*3600C= ENSP00000505655.1:n.*3600C=
ENST00000680211.1:c.819C= ENSP00000506102.1:p.Ala273=
ENST00000680280.1:n.1721C=
ENST00000680349.1:n.2867C=
ENST00000680403.1:c.4203C= ENSP00000505677.1:p.Ala1401=
ENST00000680564.1:c.3969C= ENSP00000505582.1:p.Ala1323=
ENST00000680590.1:c.*2598C= ENSP00000505350.1:n.*2598C=
ENST00000680597.1:c.951C=
ENST00000680739.1:c.1233C=
ENST00000680773.1:n.2719C=
ENST00000680806.1:c.*3521C= ENSP00000506418.1:n.*3521C=
ENST00000680997.1:n.2150C=
ENST00000681608.1:n.2063C=
ENST00000681625.1:c.*1550C= ENSP00000505555.1:n.*1550C=
ENST00000681648.1:n.2269C=
ENST00000270301.11:c.4203C= ENSP00000270301.6:p.Ala1401=
ENST00000401500.6:c.4218C= ENSP00000384792.1:p.Ala1406=
ENST00000587391.5:c.*4078C= ENSP00000465525.1:n.*4078C=
NM_001083961.1:c.4218C= NP_001077430.1:p.Ala1406=
NM_173636.4:c.4203C= NP_775907.4:p.Ala1401=
XM_005258809.2:c.4107C= XP_005258866.1:p.Ala1369=
XM_011526837.1:c.4203C= XP_011525139.1:p.Ala1401=
XM_011526838.1:c.3969C= XP_011525140.1:p.Ala1323=
XM_011526839.1:c.3867C= XP_011525141.1:p.Ala1289=
XM_011526840.1:c.3210C= XP_011525142.1:p.Ala1070=
XM_011526841.1:c.2796C= XP_011525143.1:p.Ala932=
XM_011526842.1:c.2649C= XP_011525144.1:p.Ala883=
XM_011526843.1:c.1965C= XP_011525145.1:p.Ala655=
XM_011526844.1:c.1965C= XP_011525146.1:p.Ala655=
XM_011526840.2:c.3210C= XP_011525142.1:p.Ala1070=
XM_011526841.2:c.2796C= XP_011525143.1:p.Ala932=
XM_011526844.2:c.1965C= XP_011525146.1:p.Ala655=
XM_017026665.1:c.4218C= XP_016882154.1:p.Ala1406=
NM_001083961.2:c.4218C= MANE Select NP_001077430.1:p.Ala1406=
NM_173636.5:c.4203C= NP_775907.4:p.Ala1401=