Canonical Allele Identifier: CA2584645218

Gene: WDR62

Linked Data

• gnomAD v4: 19-36104607-A-AGCAGGGTGGGGAACATCTTGC

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36104608_36104628dup , CM000681.2:g.36104608_36104628dup	GRCh38
NC_000019.9:g.36595510_36595530dup , CM000681.1:g.36595510_36595530dup	GRCh37
NC_000019.8:g.41287350_41287370dup	NCBI36
NG_028101.1:g.54728_54748dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.4229_4249dup	ENSP00000270301.6:p.Leu1416_His1417insArgArgValGlyAsnIleLeu
ENST00000401500.7:c.4244_4264dup MANE Select	ENSP00000384792.1:p.Leu1421_His1422insArgArgValGlyAsnIleLeu
ENST00000587391.6:c.*4104_*4124dup	ENSP00000465525.1:n.*4104_*4124dup
ENST00000679357.1:c.2324_2344dup
ENST00000679598.1:c.989_1009dup
ENST00000679682.1:c.4229_4249dup	ENSP00000506226.1:p.Leu1416_His1417insArgArgValGlyAsnIleLeu
ENST00000679714.1:c.4238_4258dup	ENSP00000506627.1:p.Leu1419_His1420insArgArgValGlyAsnIleLeu
ENST00000679757.1:c.3893_3913dup	ENSP00000505158.1:p.Leu1304_His1305insArgArgValGlyAsnIleLeu
ENST00000679858.1:c.*3626_*3646dup	ENSP00000505655.1:n.*3626_*3646dup
ENST00000680211.1:c.845_865dup	ENSP00000506102.1:p.Leu288_His289insArgArgValGlyAsnIleLeu
ENST00000680280.1:n.1747_1767dup
ENST00000680349.1:n.2893_2913dup
ENST00000680403.1:c.4229_4249dup	ENSP00000505677.1:p.Leu1416_His1417insArgArgValGlyAsnIleLeu
ENST00000680564.1:c.3995_4015dup	ENSP00000505582.1:p.Leu1338_His1339insArgArgValGlyAsnIleLeu
ENST00000680590.1:c.*2624_*2644dup	ENSP00000505350.1:n.*2624_*2644dup
ENST00000680597.1:c.977_997dup
ENST00000680739.1:c.1259_1279dup
ENST00000680773.1:n.2745_2765dup
ENST00000680806.1:c.*3547_*3567dup	ENSP00000506418.1:n.*3547_*3567dup
ENST00000680997.1:n.2176_2196dup
ENST00000681608.1:n.2089_2109dup
ENST00000681625.1:c.*1576_*1596dup	ENSP00000505555.1:n.*1576_*1596dup
ENST00000681648.1:n.2295_2315dup
ENST00000270301.11:c.4229_4249dup	ENSP00000270301.6:p.Leu1416_His1417insArgArgValGlyAsnIleLeu
ENST00000401500.6:c.4244_4264dup	ENSP00000384792.1:p.Leu1421_His1422insArgArgValGlyAsnIleLeu
ENST00000587391.5:c.*4104_*4124dup	ENSP00000465525.1:n.*4104_*4124dup
NM_001083961.1:c.4244_4264dup	NP_001077430.1:p.Leu1421_His1422insArgArgValGlyAsnIleLeu
NM_173636.4:c.4229_4249dup	NP_775907.4:p.Leu1416_His1417insArgArgValGlyAsnIleLeu
XM_005258809.2:c.4133_4153dup	XP_005258866.1:p.Leu1384_His1385insArgArgValGlyAsnIleLeu
XM_011526837.1:c.4229_4249dup	XP_011525139.1:p.Leu1416_His1417insArgArgValGlyAsnIleLeu
XM_011526838.1:c.3995_4015dup	XP_011525140.1:p.Leu1338_His1339insArgArgValGlyAsnIleLeu
XM_011526839.1:c.3893_3913dup	XP_011525141.1:p.Leu1304_His1305insArgArgValGlyAsnIleLeu
XM_011526840.1:c.3236_3256dup	XP_011525142.1:p.Leu1085_His1086insArgArgValGlyAsnIleLeu
XM_011526841.1:c.2822_2842dup	XP_011525143.1:p.Leu947_His948insArgArgValGlyAsnIleLeu
XM_011526842.1:c.2675_2695dup	XP_011525144.1:p.Leu898_His899insArgArgValGlyAsnIleLeu
XM_011526843.1:c.1991_2011dup	XP_011525145.1:p.Leu670_His671insArgArgValGlyAsnIleLeu
XM_011526844.1:c.1991_2011dup	XP_011525146.1:p.Leu670_His671insArgArgValGlyAsnIleLeu
XM_011526840.2:c.3236_3256dup	XP_011525142.1:p.Leu1085_His1086insArgArgValGlyAsnIleLeu
XM_011526841.2:c.2822_2842dup	XP_011525143.1:p.Leu947_His948insArgArgValGlyAsnIleLeu
XM_011526844.2:c.1991_2011dup	XP_011525146.1:p.Leu670_His671insArgArgValGlyAsnIleLeu
XM_017026665.1:c.4244_4264dup	XP_016882154.1:p.Leu1421_His1422insArgArgValGlyAsnIleLeu
NM_001083961.2:c.4244_4264dup MANE Select	NP_001077430.1:p.Leu1421_His1422insArgArgValGlyAsnIleLeu
NM_173636.5:c.4229_4249dup	NP_775907.4:p.Leu1416_His1417insArgArgValGlyAsnIleLeu