Canonical Allele Identifier: CA2333972183
Gene: WDR62 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.36104540C= , CM000681.2:g.36104540C= GRCh38
NC_000019.9:g.36595442C= , CM000681.1:g.36595442C= GRCh37
NC_000019.8:g.41287282C= NCBI36
NG_028101.1:g.54660C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000270301.12:c.4161C= ENSP00000270301.6:p.Gly1387=
ENST00000401500.7:c.4176C= MANE Select ENSP00000384792.1:p.Gly1392=
ENST00000587391.6:c.*4036C= ENSP00000465525.1:n.*4036C=
ENST00000679357.1:c.2256C=
ENST00000679598.1:c.921C=
ENST00000679682.1:c.4161C= ENSP00000506226.1:p.Gly1387=
ENST00000679714.1:c.4170C= ENSP00000506627.1:p.Gly1390=
ENST00000679757.1:c.3825C= ENSP00000505158.1:p.Gly1275=
ENST00000679858.1:c.*3558C= ENSP00000505655.1:n.*3558C=
ENST00000680211.1:c.777C= ENSP00000506102.1:p.Gly259=
ENST00000680280.1:n.1679C=
ENST00000680349.1:n.2825C=
ENST00000680403.1:c.4161C= ENSP00000505677.1:p.Gly1387=
ENST00000680564.1:c.3927C= ENSP00000505582.1:p.Gly1309=
ENST00000680590.1:c.*2556C= ENSP00000505350.1:n.*2556C=
ENST00000680597.1:c.909C=
ENST00000680739.1:c.1191C=
ENST00000680773.1:n.2677C=
ENST00000680806.1:c.*3479C= ENSP00000506418.1:n.*3479C=
ENST00000680997.1:n.2108C=
ENST00000681608.1:n.2021C=
ENST00000681625.1:c.*1508C= ENSP00000505555.1:n.*1508C=
ENST00000681648.1:n.2227C=
ENST00000270301.11:c.4161C= ENSP00000270301.6:p.Gly1387=
ENST00000401500.6:c.4176C= ENSP00000384792.1:p.Gly1392=
ENST00000587391.5:c.*4036C= ENSP00000465525.1:n.*4036C=
NM_001083961.1:c.4176C= NP_001077430.1:p.Gly1392=
NM_173636.4:c.4161C= NP_775907.4:p.Gly1387=
XM_005258809.2:c.4065C= XP_005258866.1:p.Gly1355=
XM_011526837.1:c.4161C= XP_011525139.1:p.Gly1387=
XM_011526838.1:c.3927C= XP_011525140.1:p.Gly1309=
XM_011526839.1:c.3825C= XP_011525141.1:p.Gly1275=
XM_011526840.1:c.3168C= XP_011525142.1:p.Gly1056=
XM_011526841.1:c.2754C= XP_011525143.1:p.Gly918=
XM_011526842.1:c.2607C= XP_011525144.1:p.Gly869=
XM_011526843.1:c.1923C= XP_011525145.1:p.Gly641=
XM_011526844.1:c.1923C= XP_011525146.1:p.Gly641=
XM_011526840.2:c.3168C= XP_011525142.1:p.Gly1056=
XM_011526841.2:c.2754C= XP_011525143.1:p.Gly918=
XM_011526844.2:c.1923C= XP_011525146.1:p.Gly641=
XM_017026665.1:c.4176C= XP_016882154.1:p.Gly1392=
NM_001083961.2:c.4176C= MANE Select NP_001077430.1:p.Gly1392=
NM_173636.5:c.4161C= NP_775907.4:p.Gly1387=