Canonical Allele Identifier: CA2838214767

Gene: WDR62

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36101769del , CM000681.2:g.36101769del	GRCh38
NC_000019.9:g.36592671del , CM000681.1:g.36592671del	GRCh37
NC_000019.8:g.41284511del	NCBI36
NG_028101.1:g.51889del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.3077del	ENSP00000270301.6:p.Phe1026SerfsTer?
ENST00000401500.7:c.3077del MANE Select	ENSP00000384792.1:p.Phe1026SerfsTer?
ENST00000587391.6:c.*2113del	ENSP00000465525.1:n.*2113del
ENST00000679357.1:c.867del
ENST00000679422.1:c.762-245del
ENST00000679682.1:c.3062del	ENSP00000506226.1:p.Phe1021SerfsTer?
ENST00000679714.1:c.3071del	ENSP00000506627.1:p.Phe1024SerfsTer?
ENST00000679757.1:c.2726del	ENSP00000505158.1:p.Phe909SerfsTer?
ENST00000679858.1:c.*2220del	ENSP00000505655.1:n.*2220del
ENST00000680211.1:c.-323del	ENSP00000506102.1:n.-323del
ENST00000680349.1:n.1060del
ENST00000680403.1:c.3077del	ENSP00000505677.1:p.Phe1026SerfsTer?
ENST00000680564.1:c.2971+452del	ENSP00000505582.1:n.2971+452del
ENST00000680590.1:c.*1472del	ENSP00000505350.1:n.*1472del
ENST00000680773.1:n.754del
ENST00000680806.1:c.*1801-245del	ENSP00000506418.1:n.*1801-245del
ENST00000680997.1:n.424del
ENST00000681088.1:c.739del
ENST00000681608.1:n.25del
ENST00000681625.1:c.*409del	ENSP00000505555.1:n.*409del
ENST00000270301.11:c.3077del	ENSP00000270301.6:p.Phe1026SerfsTer?
ENST00000401500.6:c.3077del	ENSP00000384792.1:p.Phe1026SerfsTer?
ENST00000587391.5:c.*2113del	ENSP00000465525.1:n.*2113del
NM_001083961.1:c.3077del	NP_001077430.1:p.Phe1026SerfsTer?
NM_173636.4:c.3077del	NP_775907.4:p.Phe1026SerfsTer?
XM_005258809.2:c.2972-245del	XP_005258866.1:n.2972-245del
XM_011526837.1:c.3062del	XP_011525139.1:p.Phe1021SerfsTer?
XM_011526838.1:c.2971+452del	XP_011525140.1:n.2971+452del
XM_011526839.1:c.2726del	XP_011525141.1:p.Phe909SerfsTer?
XM_011526840.1:c.2069del	XP_011525142.1:p.Phe690SerfsTer?
XM_011526841.1:c.1655del	XP_011525143.1:p.Phe552SerfsTer?
XM_011526842.1:c.1508del	XP_011525144.1:p.Phe503SerfsTer?
XM_011526843.1:c.824del	XP_011525145.1:p.Phe275SerfsTer?
XM_011526844.1:c.824del	XP_011525146.1:p.Phe275SerfsTer?
XM_011526840.2:c.2069del	XP_011525142.1:p.Phe690SerfsTer?
XM_011526841.2:c.1655del	XP_011525143.1:p.Phe552SerfsTer?
XM_011526844.2:c.824del	XP_011525146.1:p.Phe275SerfsTer?
XM_017026665.1:c.3077del	XP_016882154.1:p.Phe1026SerfsTer?
NM_001083961.2:c.3077del MANE Select	NP_001077430.1:p.Phe1026SerfsTer?
NM_173636.5:c.3077del	NP_775907.4:p.Phe1026SerfsTer?