Canonical Allele Identifier: CA2584644443

Gene: WDR62

Linked Data

• gnomAD v4: 19-36102146-G-GC

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36102147dup , CM000681.2:g.36102147dup	GRCh38
NC_000019.9:g.36593049dup , CM000681.1:g.36593049dup	GRCh37
NC_000019.8:g.41284889dup	NCBI36
NG_028101.1:g.52267dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.3216dup	ENSP00000270301.6:p.Arg1073GlnfsTer10
ENST00000401500.7:c.3216dup MANE Select	ENSP00000384792.1:p.Arg1073GlnfsTer15
ENST00000587391.6:c.*2491dup	ENSP00000465525.1:n.*2491dup
ENST00000679357.1:c.1006dup
ENST00000679422.1:c.895dup
ENST00000679682.1:c.3201dup	ENSP00000506226.1:p.Arg1068GlnfsTer15
ENST00000679714.1:c.3210dup	ENSP00000506627.1:p.Arg1071GlnfsTer15
ENST00000679757.1:c.2865dup	ENSP00000505158.1:p.Arg956GlnfsTer15
ENST00000679858.1:c.*2598dup	ENSP00000505655.1:n.*2598dup
ENST00000680211.1:c.-184dup	ENSP00000506102.1:n.-184dup
ENST00000680349.1:n.1199dup
ENST00000680403.1:c.3216dup	ENSP00000505677.1:p.Arg1073GlnfsTer10
ENST00000680564.1:c.2972-590dup	ENSP00000505582.1:n.2972-590dup
ENST00000680590.1:c.*1611dup	ENSP00000505350.1:n.*1611dup
ENST00000680739.1:c.134dup
ENST00000680773.1:n.1132dup
ENST00000680806.1:c.*1934dup	ENSP00000506418.1:n.*1934dup
ENST00000680997.1:n.563dup
ENST00000681088.1:c.878dup
ENST00000681608.1:n.164dup
ENST00000681625.1:c.*548dup	ENSP00000505555.1:n.*548dup
ENST00000270301.11:c.3216dup	ENSP00000270301.6:p.Arg1073GlnfsTer10
ENST00000401500.6:c.3216dup	ENSP00000384792.1:p.Arg1073GlnfsTer15
ENST00000587391.5:c.*2491dup	ENSP00000465525.1:n.*2491dup
NM_001083961.1:c.3216dup	NP_001077430.1:p.Arg1073GlnfsTer15
NM_173636.4:c.3216dup	NP_775907.4:p.Arg1073GlnfsTer10
XM_005258809.2:c.3105dup	XP_005258866.1:p.Arg1036GlnfsTer15
XM_011526837.1:c.3201dup	XP_011525139.1:p.Arg1068GlnfsTer15
XM_011526838.1:c.2972-590dup	XP_011525140.1:n.2972-590dup
XM_011526839.1:c.2865dup	XP_011525141.1:p.Arg956GlnfsTer15
XM_011526840.1:c.2208dup	XP_011525142.1:p.Arg737GlnfsTer15
XM_011526841.1:c.1794dup	XP_011525143.1:p.Arg599GlnfsTer15
XM_011526842.1:c.1647dup	XP_011525144.1:p.Arg550GlnfsTer15
XM_011526843.1:c.963dup	XP_011525145.1:p.Arg322GlnfsTer15
XM_011526844.1:c.963dup	XP_011525146.1:p.Arg322GlnfsTer15
XM_011526840.2:c.2208dup	XP_011525142.1:p.Arg737GlnfsTer15
XM_011526841.2:c.1794dup	XP_011525143.1:p.Arg599GlnfsTer15
XM_011526844.2:c.963dup	XP_011525146.1:p.Arg322GlnfsTer15
XM_017026665.1:c.3216dup	XP_016882154.1:p.Arg1073GlnfsTer15
NM_001083961.2:c.3216dup MANE Select	NP_001077430.1:p.Arg1073GlnfsTer15
NM_173636.5:c.3216dup	NP_775907.4:p.Arg1073GlnfsTer10