Canonical Allele Identifier: CA2333970928
Gene: WDR62 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.36102079C= , CM000681.2:g.36102079C= GRCh38
NC_000019.9:g.36592981C= , CM000681.1:g.36592981C= GRCh37
NC_000019.8:g.41284821C= NCBI36
NG_028101.1:g.52199C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000270301.12:c.3148C= ENSP00000270301.6:p.Leu1050=
ENST00000401500.7:c.3148C= MANE Select ENSP00000384792.1:p.Leu1050=
ENST00000587391.6:c.*2423C= ENSP00000465525.1:n.*2423C=
ENST00000679357.1:c.938C=
ENST00000679422.1:c.827C=
ENST00000679682.1:c.3133C= ENSP00000506226.1:p.Leu1045=
ENST00000679714.1:c.3142C= ENSP00000506627.1:p.Leu1048=
ENST00000679757.1:c.2797C= ENSP00000505158.1:p.Leu933=
ENST00000679858.1:c.*2530C= ENSP00000505655.1:n.*2530C=
ENST00000680211.1:c.-252C= ENSP00000506102.1:n.-252C=
ENST00000680349.1:n.1131C=
ENST00000680403.1:c.3148C= ENSP00000505677.1:p.Leu1050=
ENST00000680564.1:c.2972-658C= ENSP00000505582.1:n.2972-658C=
ENST00000680590.1:c.*1543C= ENSP00000505350.1:n.*1543C=
ENST00000680739.1:c.66C=
ENST00000680773.1:n.1064C=
ENST00000680806.1:c.*1866C= ENSP00000506418.1:n.*1866C=
ENST00000680997.1:n.495C=
ENST00000681088.1:c.810C=
ENST00000681608.1:n.96C=
ENST00000681625.1:c.*480C= ENSP00000505555.1:n.*480C=
ENST00000270301.11:c.3148C= ENSP00000270301.6:p.Leu1050=
ENST00000401500.6:c.3148C= ENSP00000384792.1:p.Leu1050=
ENST00000587391.5:c.*2423C= ENSP00000465525.1:n.*2423C=
NM_001083961.1:c.3148C= NP_001077430.1:p.Leu1050=
NM_173636.4:c.3148C= NP_775907.4:p.Leu1050=
XM_005258809.2:c.3037C= XP_005258866.1:p.Leu1013=
XM_011526837.1:c.3133C= XP_011525139.1:p.Leu1045=
XM_011526838.1:c.2972-658C= XP_011525140.1:n.2972-658C=
XM_011526839.1:c.2797C= XP_011525141.1:p.Leu933=
XM_011526840.1:c.2140C= XP_011525142.1:p.Leu714=
XM_011526841.1:c.1726C= XP_011525143.1:p.Leu576=
XM_011526842.1:c.1579C= XP_011525144.1:p.Leu527=
XM_011526843.1:c.895C= XP_011525145.1:p.Leu299=
XM_011526844.1:c.895C= XP_011525146.1:p.Leu299=
XM_011526840.2:c.2140C= XP_011525142.1:p.Leu714=
XM_011526841.2:c.1726C= XP_011525143.1:p.Leu576=
XM_011526844.2:c.895C= XP_011525146.1:p.Leu299=
XM_017026665.1:c.3148C= XP_016882154.1:p.Leu1050=
NM_001083961.2:c.3148C= MANE Select NP_001077430.1:p.Leu1050=
NM_173636.5:c.3148C= NP_775907.4:p.Leu1050=