Canonical Allele Identifier: CA2584644440

Gene: WDR62

Linked Data

• gnomAD v4: 19-36102120-C-CT

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36102123dup , CM000681.2:g.36102123dup	GRCh38
NC_000019.9:g.36593025dup , CM000681.1:g.36593025dup	GRCh37
NC_000019.8:g.41284865dup	NCBI36
NG_028101.1:g.52243dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.3192dup	ENSP00000270301.6:p.Glu1065Ter
ENST00000401500.7:c.3192dup MANE Select	ENSP00000384792.1:p.Glu1065Ter
ENST00000587391.6:c.*2467dup	ENSP00000465525.1:n.*2467dup
ENST00000679357.1:c.982dup
ENST00000679422.1:c.871dup
ENST00000679682.1:c.3177dup	ENSP00000506226.1:p.Glu1060Ter
ENST00000679714.1:c.3186dup	ENSP00000506627.1:p.Glu1063Ter
ENST00000679757.1:c.2841dup	ENSP00000505158.1:p.Glu948Ter
ENST00000679858.1:c.*2574dup	ENSP00000505655.1:n.*2574dup
ENST00000680211.1:c.-208dup	ENSP00000506102.1:n.-208dup
ENST00000680349.1:n.1175dup
ENST00000680403.1:c.3192dup	ENSP00000505677.1:p.Glu1065Ter
ENST00000680564.1:c.2972-614dup	ENSP00000505582.1:n.2972-614dup
ENST00000680590.1:c.*1587dup	ENSP00000505350.1:n.*1587dup
ENST00000680739.1:c.110dup
ENST00000680773.1:n.1108dup
ENST00000680806.1:c.*1910dup	ENSP00000506418.1:n.*1910dup
ENST00000680997.1:n.539dup
ENST00000681088.1:c.854dup
ENST00000681608.1:n.140dup
ENST00000681625.1:c.*524dup	ENSP00000505555.1:n.*524dup
ENST00000270301.11:c.3192dup	ENSP00000270301.6:p.Glu1065Ter
ENST00000401500.6:c.3192dup	ENSP00000384792.1:p.Glu1065Ter
ENST00000587391.5:c.*2467dup	ENSP00000465525.1:n.*2467dup
NM_001083961.1:c.3192dup	NP_001077430.1:p.Glu1065Ter
NM_173636.4:c.3192dup	NP_775907.4:p.Glu1065Ter
XM_005258809.2:c.3081dup	XP_005258866.1:p.Glu1028Ter
XM_011526837.1:c.3177dup	XP_011525139.1:p.Glu1060Ter
XM_011526838.1:c.2972-614dup	XP_011525140.1:n.2972-614dup
XM_011526839.1:c.2841dup	XP_011525141.1:p.Glu948Ter
XM_011526840.1:c.2184dup	XP_011525142.1:p.Glu729Ter
XM_011526841.1:c.1770dup	XP_011525143.1:p.Glu591Ter
XM_011526842.1:c.1623dup	XP_011525144.1:p.Glu542Ter
XM_011526843.1:c.939dup	XP_011525145.1:p.Glu314Ter
XM_011526844.1:c.939dup	XP_011525146.1:p.Glu314Ter
XM_011526840.2:c.2184dup	XP_011525142.1:p.Glu729Ter
XM_011526841.2:c.1770dup	XP_011525143.1:p.Glu591Ter
XM_011526844.2:c.939dup	XP_011525146.1:p.Glu314Ter
XM_017026665.1:c.3192dup	XP_016882154.1:p.Glu1065Ter
NM_001083961.2:c.3192dup MANE Select	NP_001077430.1:p.Glu1065Ter
NM_173636.5:c.3192dup	NP_775907.4:p.Glu1065Ter