Canonical Allele Identifier: CA2842387267
Gene: WDR62 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.36102771dup , CM000681.2:g.36102771dup GRCh38
NC_000019.9:g.36593673dup , CM000681.1:g.36593673dup GRCh37
NC_000019.8:g.41285513dup NCBI36
NG_028101.1:g.52891dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000270301.12:c.3240dup ENSP00000270301.6:p.Ser1081LeufsTer2
ENST00000401500.7:c.3255dup MANE Select ENSP00000384792.1:p.Ser1086LeufsTer2
ENST00000587391.6:c.*3115dup ENSP00000465525.1:n.*3115dup
ENST00000679357.1:c.1335dup
ENST00000679598.1:c.20dup
ENST00000679682.1:c.3240dup ENSP00000506226.1:p.Ser1081LeufsTer2
ENST00000679714.1:c.3249dup ENSP00000506627.1:p.Ser1084LeufsTer2
ENST00000679757.1:c.2904dup ENSP00000505158.1:p.Ser969LeufsTer2
ENST00000679858.1:c.*2637dup ENSP00000505655.1:n.*2637dup
ENST00000680211.1:c.-145dup ENSP00000506102.1:n.-145dup
ENST00000680280.1:n.542dup
ENST00000680349.1:n.1823dup
ENST00000680403.1:c.3240dup ENSP00000505677.1:p.Ser1081LeufsTer2
ENST00000680564.1:c.3006dup ENSP00000505582.1:p.Ser1003LeufsTer2
ENST00000680590.1:c.*1635dup ENSP00000505350.1:n.*1635dup
ENST00000680597.1:c.20dup
ENST00000680739.1:c.270dup
ENST00000680773.1:n.1756dup
ENST00000680806.1:c.*2558dup ENSP00000506418.1:n.*2558dup
ENST00000680997.1:n.1187dup
ENST00000681608.1:n.788dup
ENST00000681625.1:c.*587dup ENSP00000505555.1:n.*587dup
ENST00000681648.1:n.554dup
ENST00000270301.11:c.3240dup ENSP00000270301.6:p.Ser1081LeufsTer2
ENST00000401500.6:c.3255dup ENSP00000384792.1:p.Ser1086LeufsTer2
ENST00000587391.5:c.*3115dup ENSP00000465525.1:n.*3115dup
NM_001083961.1:c.3255dup NP_001077430.1:p.Ser1086LeufsTer2
NM_173636.4:c.3240dup NP_775907.4:p.Ser1081LeufsTer2
XM_005258809.2:c.3144dup XP_005258866.1:p.Ser1049LeufsTer2
XM_011526837.1:c.3240dup XP_011525139.1:p.Ser1081LeufsTer2
XM_011526838.1:c.3006dup XP_011525140.1:p.Ser1003LeufsTer2
XM_011526839.1:c.2904dup XP_011525141.1:p.Ser969LeufsTer2
XM_011526840.1:c.2247dup XP_011525142.1:p.Ser750LeufsTer2
XM_011526841.1:c.1833dup XP_011525143.1:p.Ser612LeufsTer2
XM_011526842.1:c.1686dup XP_011525144.1:p.Ser563LeufsTer2
XM_011526843.1:c.1002dup XP_011525145.1:p.Ser335LeufsTer2
XM_011526844.1:c.1002dup XP_011525146.1:p.Ser335LeufsTer2
XM_011526840.2:c.2247dup XP_011525142.1:p.Ser750LeufsTer2
XM_011526841.2:c.1833dup XP_011525143.1:p.Ser612LeufsTer2
XM_011526844.2:c.1002dup XP_011525146.1:p.Ser335LeufsTer2
XM_017026665.1:c.3255dup XP_016882154.1:p.Ser1086LeufsTer2
NM_001083961.2:c.3255dup MANE Select NP_001077430.1:p.Ser1086LeufsTer2
NM_173636.5:c.3240dup NP_775907.4:p.Ser1081LeufsTer2