Canonical Allele Identifier: CA2333970926
Gene: WDR62 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.36102074G= , CM000681.2:g.36102074G= GRCh38
NC_000019.9:g.36592976G= , CM000681.1:g.36592976G= GRCh37
NC_000019.8:g.41284816G= NCBI36
NG_028101.1:g.52194G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000270301.12:c.3143G= ENSP00000270301.6:p.Ser1048=
ENST00000401500.7:c.3143G= MANE Select ENSP00000384792.1:p.Ser1048=
ENST00000587391.6:c.*2418G= ENSP00000465525.1:n.*2418G=
ENST00000679357.1:c.933G=
ENST00000679422.1:c.822G=
ENST00000679682.1:c.3128G= ENSP00000506226.1:p.Ser1043=
ENST00000679714.1:c.3137G= ENSP00000506627.1:p.Ser1046=
ENST00000679757.1:c.2792G= ENSP00000505158.1:p.Ser931=
ENST00000679858.1:c.*2525G= ENSP00000505655.1:n.*2525G=
ENST00000680211.1:c.-257G= ENSP00000506102.1:n.-257G=
ENST00000680349.1:n.1126G=
ENST00000680403.1:c.3143G= ENSP00000505677.1:p.Ser1048=
ENST00000680564.1:c.2972-663G= ENSP00000505582.1:n.2972-663G=
ENST00000680590.1:c.*1538G= ENSP00000505350.1:n.*1538G=
ENST00000680739.1:c.61G=
ENST00000680773.1:n.1059G=
ENST00000680806.1:c.*1861G= ENSP00000506418.1:n.*1861G=
ENST00000680997.1:n.490G=
ENST00000681088.1:c.805G=
ENST00000681608.1:n.91G=
ENST00000681625.1:c.*475G= ENSP00000505555.1:n.*475G=
ENST00000270301.11:c.3143G= ENSP00000270301.6:p.Ser1048=
ENST00000401500.6:c.3143G= ENSP00000384792.1:p.Ser1048=
ENST00000587391.5:c.*2418G= ENSP00000465525.1:n.*2418G=
NM_001083961.1:c.3143G= NP_001077430.1:p.Ser1048=
NM_173636.4:c.3143G= NP_775907.4:p.Ser1048=
XM_005258809.2:c.3032G= XP_005258866.1:p.Ser1011=
XM_011526837.1:c.3128G= XP_011525139.1:p.Ser1043=
XM_011526838.1:c.2972-663G= XP_011525140.1:n.2972-663G=
XM_011526839.1:c.2792G= XP_011525141.1:p.Ser931=
XM_011526840.1:c.2135G= XP_011525142.1:p.Ser712=
XM_011526841.1:c.1721G= XP_011525143.1:p.Ser574=
XM_011526842.1:c.1574G= XP_011525144.1:p.Ser525=
XM_011526843.1:c.890G= XP_011525145.1:p.Ser297=
XM_011526844.1:c.890G= XP_011525146.1:p.Ser297=
XM_011526840.2:c.2135G= XP_011525142.1:p.Ser712=
XM_011526841.2:c.1721G= XP_011525143.1:p.Ser574=
XM_011526844.2:c.890G= XP_011525146.1:p.Ser297=
XM_017026665.1:c.3143G= XP_016882154.1:p.Ser1048=
NM_001083961.2:c.3143G= MANE Select NP_001077430.1:p.Ser1048=
NM_173636.5:c.3143G= NP_775907.4:p.Ser1048=