Canonical Allele Identifier: CA2736057245
Gene: WDR62 HGNC NCBI

Linked Data

dbSNP Id: rs2145865733

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.36102069del , CM000681.2:g.36102069del GRCh38
NC_000019.9:g.36592971del , CM000681.1:g.36592971del GRCh37
NC_000019.8:g.41284811del NCBI36
NG_028101.1:g.52189del

Transcript Alleles

HGVS Amino-acid Change
ENST00000270301.12:c.3138del ENSP00000270301.6:p.Ser1047AlafsTer21
ENST00000401500.7:c.3138del MANE Select ENSP00000384792.1:p.Ser1047AlafsTer21
ENST00000587391.6:c.*2413del ENSP00000465525.1:n.*2413del
ENST00000679357.1:c.928del
ENST00000679422.1:c.817del
ENST00000679682.1:c.3123del ENSP00000506226.1:p.Ser1042AlafsTer21
ENST00000679714.1:c.3132del ENSP00000506627.1:p.Ser1045AlafsTer21
ENST00000679757.1:c.2787del ENSP00000505158.1:p.Ser930AlafsTer21
ENST00000679858.1:c.*2520del ENSP00000505655.1:n.*2520del
ENST00000680211.1:c.-262del ENSP00000506102.1:n.-262del
ENST00000680349.1:n.1121del
ENST00000680403.1:c.3138del ENSP00000505677.1:p.Ser1047AlafsTer21
ENST00000680564.1:c.2972-668del ENSP00000505582.1:n.2972-668del
ENST00000680590.1:c.*1533del ENSP00000505350.1:n.*1533del
ENST00000680739.1:c.56del
ENST00000680773.1:n.1054del
ENST00000680806.1:c.*1856del ENSP00000506418.1:n.*1856del
ENST00000680997.1:n.485del
ENST00000681088.1:c.800del
ENST00000681608.1:n.86del
ENST00000681625.1:c.*470del ENSP00000505555.1:n.*470del
ENST00000270301.11:c.3138del ENSP00000270301.6:p.Ser1047AlafsTer21
ENST00000401500.6:c.3138del ENSP00000384792.1:p.Ser1047AlafsTer21
ENST00000587391.5:c.*2413del ENSP00000465525.1:n.*2413del
NM_001083961.1:c.3138del NP_001077430.1:p.Ser1047AlafsTer21
NM_173636.4:c.3138del NP_775907.4:p.Ser1047AlafsTer21
XM_005258809.2:c.3027del XP_005258866.1:p.Ser1010AlafsTer21
XM_011526837.1:c.3123del XP_011525139.1:p.Ser1042AlafsTer21
XM_011526838.1:c.2972-668del XP_011525140.1:n.2972-668del
XM_011526839.1:c.2787del XP_011525141.1:p.Ser930AlafsTer21
XM_011526840.1:c.2130del XP_011525142.1:p.Ser711AlafsTer21
XM_011526841.1:c.1716del XP_011525143.1:p.Ser573AlafsTer21
XM_011526842.1:c.1569del XP_011525144.1:p.Ser524AlafsTer21
XM_011526843.1:c.885del XP_011525145.1:p.Ser296AlafsTer21
XM_011526844.1:c.885del XP_011525146.1:p.Ser296AlafsTer21
XM_011526840.2:c.2130del XP_011525142.1:p.Ser711AlafsTer21
XM_011526841.2:c.1716del XP_011525143.1:p.Ser573AlafsTer21
XM_011526844.2:c.885del XP_011525146.1:p.Ser296AlafsTer21
XM_017026665.1:c.3138del XP_016882154.1:p.Ser1047AlafsTer21
NM_001083961.2:c.3138del MANE Select NP_001077430.1:p.Ser1047AlafsTer21
NM_173636.5:c.3138del NP_775907.4:p.Ser1047AlafsTer21