Canonical Allele Identifier: CA2333972228
Gene: WDR62 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.36104634C= , CM000681.2:g.36104634C= GRCh38
NC_000019.9:g.36595536C= , CM000681.1:g.36595536C= GRCh37
NC_000019.8:g.41287376C= NCBI36
NG_028101.1:g.54754C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000270301.12:c.4255C= ENSP00000270301.6:p.Leu1419=
ENST00000401500.7:c.4270C= MANE Select ENSP00000384792.1:p.Leu1424=
ENST00000587391.6:c.*4130C= ENSP00000465525.1:n.*4130C=
ENST00000679357.1:c.2350C=
ENST00000679598.1:c.1015C=
ENST00000679682.1:c.4255C= ENSP00000506226.1:p.Leu1419=
ENST00000679714.1:c.4264C= ENSP00000506627.1:p.Leu1422=
ENST00000679757.1:c.3919C= ENSP00000505158.1:p.Leu1307=
ENST00000679858.1:c.*3652C= ENSP00000505655.1:n.*3652C=
ENST00000680211.1:c.871C= ENSP00000506102.1:p.Leu291=
ENST00000680280.1:n.1773C=
ENST00000680349.1:n.2919C=
ENST00000680403.1:c.4255C= ENSP00000505677.1:p.Leu1419=
ENST00000680564.1:c.4021C= ENSP00000505582.1:p.Leu1341=
ENST00000680590.1:c.*2650C= ENSP00000505350.1:n.*2650C=
ENST00000680597.1:c.1003C=
ENST00000680739.1:c.1285C=
ENST00000680773.1:n.2771C=
ENST00000680806.1:c.*3573C= ENSP00000506418.1:n.*3573C=
ENST00000680997.1:n.2202C=
ENST00000681608.1:n.2115C=
ENST00000681625.1:c.*1602C= ENSP00000505555.1:n.*1602C=
ENST00000681648.1:n.2321C=
ENST00000270301.11:c.4255C= ENSP00000270301.6:p.Leu1419=
ENST00000401500.6:c.4270C= ENSP00000384792.1:p.Leu1424=
ENST00000587391.5:c.*4130C= ENSP00000465525.1:n.*4130C=
NM_001083961.1:c.4270C= NP_001077430.1:p.Leu1424=
NM_173636.4:c.4255C= NP_775907.4:p.Leu1419=
XM_005258809.2:c.4159C= XP_005258866.1:p.Leu1387=
XM_011526837.1:c.4255C= XP_011525139.1:p.Leu1419=
XM_011526838.1:c.4021C= XP_011525140.1:p.Leu1341=
XM_011526839.1:c.3919C= XP_011525141.1:p.Leu1307=
XM_011526840.1:c.3262C= XP_011525142.1:p.Leu1088=
XM_011526841.1:c.2848C= XP_011525143.1:p.Leu950=
XM_011526842.1:c.2701C= XP_011525144.1:p.Leu901=
XM_011526843.1:c.2017C= XP_011525145.1:p.Leu673=
XM_011526844.1:c.2017C= XP_011525146.1:p.Leu673=
XM_011526840.2:c.3262C= XP_011525142.1:p.Leu1088=
XM_011526841.2:c.2848C= XP_011525143.1:p.Leu950=
XM_011526844.2:c.2017C= XP_011525146.1:p.Leu673=
XM_017026665.1:c.4270C= XP_016882154.1:p.Leu1424=
NM_001083961.2:c.4270C= MANE Select NP_001077430.1:p.Leu1424=
NM_173636.5:c.4255C= NP_775907.4:p.Leu1419=