Canonical Allele Identifier: CA2333970757
Gene: WDR62 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.36101741C= , CM000681.2:g.36101741C= GRCh38
NC_000019.9:g.36592643C= , CM000681.1:g.36592643C= GRCh37
NC_000019.8:g.41284483C= NCBI36
NG_028101.1:g.51861C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000270301.12:c.3049C= ENSP00000270301.6:p.Pro1017=
ENST00000401500.7:c.3049C= MANE Select ENSP00000384792.1:p.Pro1017=
ENST00000587391.6:c.*2085C= ENSP00000465525.1:n.*2085C=
ENST00000679357.1:c.839C=
ENST00000679422.1:c.762-273C=
ENST00000679682.1:c.3034C= ENSP00000506226.1:p.Pro1012=
ENST00000679714.1:c.3043C= ENSP00000506627.1:p.Pro1015=
ENST00000679757.1:c.2698C= ENSP00000505158.1:p.Pro900=
ENST00000679858.1:c.*2192C= ENSP00000505655.1:n.*2192C=
ENST00000680211.1:c.-351C= ENSP00000506102.1:n.-351C=
ENST00000680349.1:n.1032C=
ENST00000680403.1:c.3049C= ENSP00000505677.1:p.Pro1017=
ENST00000680564.1:c.2971+424C= ENSP00000505582.1:n.2971+424C=
ENST00000680590.1:c.*1444C= ENSP00000505350.1:n.*1444C=
ENST00000680773.1:n.726C=
ENST00000680806.1:c.*1801-273C= ENSP00000506418.1:n.*1801-273C=
ENST00000680997.1:n.396C=
ENST00000681088.1:c.711C=
ENST00000681625.1:c.*381C= ENSP00000505555.1:n.*381C=
ENST00000270301.11:c.3049C= ENSP00000270301.6:p.Pro1017=
ENST00000401500.6:c.3049C= ENSP00000384792.1:p.Pro1017=
ENST00000587391.5:c.*2085C= ENSP00000465525.1:n.*2085C=
NM_001083961.1:c.3049C= NP_001077430.1:p.Pro1017=
NM_173636.4:c.3049C= NP_775907.4:p.Pro1017=
XM_005258809.2:c.2972-273C= XP_005258866.1:n.2972-273C=
XM_011526837.1:c.3034C= XP_011525139.1:p.Pro1012=
XM_011526838.1:c.2971+424C= XP_011525140.1:n.2971+424C=
XM_011526839.1:c.2698C= XP_011525141.1:p.Pro900=
XM_011526840.1:c.2041C= XP_011525142.1:p.Pro681=
XM_011526841.1:c.1627C= XP_011525143.1:p.Pro543=
XM_011526842.1:c.1480C= XP_011525144.1:p.Pro494=
XM_011526843.1:c.796C= XP_011525145.1:p.Pro266=
XM_011526844.1:c.796C= XP_011525146.1:p.Pro266=
XM_011526840.2:c.2041C= XP_011525142.1:p.Pro681=
XM_011526841.2:c.1627C= XP_011525143.1:p.Pro543=
XM_011526844.2:c.796C= XP_011525146.1:p.Pro266=
XM_017026665.1:c.3049C= XP_016882154.1:p.Pro1017=
NM_001083961.2:c.3049C= MANE Select NP_001077430.1:p.Pro1017=
NM_173636.5:c.3049C= NP_775907.4:p.Pro1017=