Canonical Allele Identifier: CA2333972186
Gene: WDR62 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.36104545C= , CM000681.2:g.36104545C= GRCh38
NC_000019.9:g.36595447C= , CM000681.1:g.36595447C= GRCh37
NC_000019.8:g.41287287C= NCBI36
NG_028101.1:g.54665C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000270301.12:c.4166C= ENSP00000270301.6:p.Pro1389=
ENST00000401500.7:c.4181C= MANE Select ENSP00000384792.1:p.Pro1394=
ENST00000587391.6:c.*4041C= ENSP00000465525.1:n.*4041C=
ENST00000679357.1:c.2261C=
ENST00000679598.1:c.926C=
ENST00000679682.1:c.4166C= ENSP00000506226.1:p.Pro1389=
ENST00000679714.1:c.4175C= ENSP00000506627.1:p.Pro1392=
ENST00000679757.1:c.3830C= ENSP00000505158.1:p.Pro1277=
ENST00000679858.1:c.*3563C= ENSP00000505655.1:n.*3563C=
ENST00000680211.1:c.782C= ENSP00000506102.1:p.Pro261=
ENST00000680280.1:n.1684C=
ENST00000680349.1:n.2830C=
ENST00000680403.1:c.4166C= ENSP00000505677.1:p.Pro1389=
ENST00000680564.1:c.3932C= ENSP00000505582.1:p.Pro1311=
ENST00000680590.1:c.*2561C= ENSP00000505350.1:n.*2561C=
ENST00000680597.1:c.914C=
ENST00000680739.1:c.1196C=
ENST00000680773.1:n.2682C=
ENST00000680806.1:c.*3484C= ENSP00000506418.1:n.*3484C=
ENST00000680997.1:n.2113C=
ENST00000681608.1:n.2026C=
ENST00000681625.1:c.*1513C= ENSP00000505555.1:n.*1513C=
ENST00000681648.1:n.2232C=
ENST00000270301.11:c.4166C= ENSP00000270301.6:p.Pro1389=
ENST00000401500.6:c.4181C= ENSP00000384792.1:p.Pro1394=
ENST00000587391.5:c.*4041C= ENSP00000465525.1:n.*4041C=
NM_001083961.1:c.4181C= NP_001077430.1:p.Pro1394=
NM_173636.4:c.4166C= NP_775907.4:p.Pro1389=
XM_005258809.2:c.4070C= XP_005258866.1:p.Pro1357=
XM_011526837.1:c.4166C= XP_011525139.1:p.Pro1389=
XM_011526838.1:c.3932C= XP_011525140.1:p.Pro1311=
XM_011526839.1:c.3830C= XP_011525141.1:p.Pro1277=
XM_011526840.1:c.3173C= XP_011525142.1:p.Pro1058=
XM_011526841.1:c.2759C= XP_011525143.1:p.Pro920=
XM_011526842.1:c.2612C= XP_011525144.1:p.Pro871=
XM_011526843.1:c.1928C= XP_011525145.1:p.Pro643=
XM_011526844.1:c.1928C= XP_011525146.1:p.Pro643=
XM_011526840.2:c.3173C= XP_011525142.1:p.Pro1058=
XM_011526841.2:c.2759C= XP_011525143.1:p.Pro920=
XM_011526844.2:c.1928C= XP_011525146.1:p.Pro643=
XM_017026665.1:c.4181C= XP_016882154.1:p.Pro1394=
NM_001083961.2:c.4181C= MANE Select NP_001077430.1:p.Pro1394=
NM_173636.5:c.4166C= NP_775907.4:p.Pro1389=