Canonical Allele Identifier: CA2333972208
Gene: WDR62 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.36104594T= , CM000681.2:g.36104594T= GRCh38
NC_000019.9:g.36595496T= , CM000681.1:g.36595496T= GRCh37
NC_000019.8:g.41287336T= NCBI36
NG_028101.1:g.54714T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000270301.12:c.4215T= ENSP00000270301.6:p.Ser1405=
ENST00000401500.7:c.4230T= MANE Select ENSP00000384792.1:p.Ser1410=
ENST00000587391.6:c.*4090T= ENSP00000465525.1:n.*4090T=
ENST00000679357.1:c.2310T=
ENST00000679598.1:c.975T=
ENST00000679682.1:c.4215T= ENSP00000506226.1:p.Ser1405=
ENST00000679714.1:c.4224T= ENSP00000506627.1:p.Ser1408=
ENST00000679757.1:c.3879T= ENSP00000505158.1:p.Ser1293=
ENST00000679858.1:c.*3612T= ENSP00000505655.1:n.*3612T=
ENST00000680211.1:c.831T= ENSP00000506102.1:p.Ser277=
ENST00000680280.1:n.1733T=
ENST00000680349.1:n.2879T=
ENST00000680403.1:c.4215T= ENSP00000505677.1:p.Ser1405=
ENST00000680564.1:c.3981T= ENSP00000505582.1:p.Ser1327=
ENST00000680590.1:c.*2610T= ENSP00000505350.1:n.*2610T=
ENST00000680597.1:c.963T=
ENST00000680739.1:c.1245T=
ENST00000680773.1:n.2731T=
ENST00000680806.1:c.*3533T= ENSP00000506418.1:n.*3533T=
ENST00000680997.1:n.2162T=
ENST00000681608.1:n.2075T=
ENST00000681625.1:c.*1562T= ENSP00000505555.1:n.*1562T=
ENST00000681648.1:n.2281T=
ENST00000270301.11:c.4215T= ENSP00000270301.6:p.Ser1405=
ENST00000401500.6:c.4230T= ENSP00000384792.1:p.Ser1410=
ENST00000587391.5:c.*4090T= ENSP00000465525.1:n.*4090T=
NM_001083961.1:c.4230T= NP_001077430.1:p.Ser1410=
NM_173636.4:c.4215T= NP_775907.4:p.Ser1405=
XM_005258809.2:c.4119T= XP_005258866.1:p.Ser1373=
XM_011526837.1:c.4215T= XP_011525139.1:p.Ser1405=
XM_011526838.1:c.3981T= XP_011525140.1:p.Ser1327=
XM_011526839.1:c.3879T= XP_011525141.1:p.Ser1293=
XM_011526840.1:c.3222T= XP_011525142.1:p.Ser1074=
XM_011526841.1:c.2808T= XP_011525143.1:p.Ser936=
XM_011526842.1:c.2661T= XP_011525144.1:p.Ser887=
XM_011526843.1:c.1977T= XP_011525145.1:p.Ser659=
XM_011526844.1:c.1977T= XP_011525146.1:p.Ser659=
XM_011526840.2:c.3222T= XP_011525142.1:p.Ser1074=
XM_011526841.2:c.2808T= XP_011525143.1:p.Ser936=
XM_011526844.2:c.1977T= XP_011525146.1:p.Ser659=
XM_017026665.1:c.4230T= XP_016882154.1:p.Ser1410=
NM_001083961.2:c.4230T= MANE Select NP_001077430.1:p.Ser1410=
NM_173636.5:c.4215T= NP_775907.4:p.Ser1405=