Canonical Allele Identifier: CA2584644438

Gene: WDR62

Linked Data

• gnomAD v4: 19-36102057-A-ACCCAGCGTC

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36102064_36102072dup , CM000681.2:g.36102064_36102072dup	GRCh38
NC_000019.9:g.36592966_36592974dup , CM000681.1:g.36592966_36592974dup	GRCh37
NC_000019.8:g.41284806_41284814dup	NCBI36
NG_028101.1:g.52184_52192dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.3133_3141dup	ENSP00000270301.6:p.Ser1047_Ser1048insValProSer
ENST00000401500.7:c.3133_3141dup MANE Select	ENSP00000384792.1:p.Ser1047_Ser1048insValProSer
ENST00000587391.6:c.*2408_*2416dup	ENSP00000465525.1:n.*2408_*2416dup
ENST00000679357.1:c.923_931dup
ENST00000679422.1:c.812_820dup
ENST00000679682.1:c.3118_3126dup	ENSP00000506226.1:p.Ser1042_Ser1043insValProSer
ENST00000679714.1:c.3127_3135dup	ENSP00000506627.1:p.Ser1045_Ser1046insValProSer
ENST00000679757.1:c.2782_2790dup	ENSP00000505158.1:p.Ser930_Ser931insValProSer
ENST00000679858.1:c.*2515_*2523dup	ENSP00000505655.1:n.*2515_*2523dup
ENST00000680211.1:c.-267_-259dup	ENSP00000506102.1:n.-267_-259dup
ENST00000680349.1:n.1116_1124dup
ENST00000680403.1:c.3133_3141dup	ENSP00000505677.1:p.Ser1047_Ser1048insValProSer
ENST00000680564.1:c.2972-673_2972-665dup	ENSP00000505582.1:n.2972-673_2972-665dup
ENST00000680590.1:c.*1528_*1536dup	ENSP00000505350.1:n.*1528_*1536dup
ENST00000680739.1:c.51_59dup
ENST00000680773.1:n.1049_1057dup
ENST00000680806.1:c.*1851_*1859dup	ENSP00000506418.1:n.*1851_*1859dup
ENST00000680997.1:n.480_488dup
ENST00000681088.1:c.795_803dup
ENST00000681608.1:n.81_89dup
ENST00000681625.1:c.*465_*473dup	ENSP00000505555.1:n.*465_*473dup
ENST00000270301.11:c.3133_3141dup	ENSP00000270301.6:p.Ser1047_Ser1048insValProSer
ENST00000401500.6:c.3133_3141dup	ENSP00000384792.1:p.Ser1047_Ser1048insValProSer
ENST00000587391.5:c.*2408_*2416dup	ENSP00000465525.1:n.*2408_*2416dup
NM_001083961.1:c.3133_3141dup	NP_001077430.1:p.Ser1047_Ser1048insValProSer
NM_173636.4:c.3133_3141dup	NP_775907.4:p.Ser1047_Ser1048insValProSer
XM_005258809.2:c.3022_3030dup	XP_005258866.1:p.Ser1010_Ser1011insValProSer
XM_011526837.1:c.3118_3126dup	XP_011525139.1:p.Ser1042_Ser1043insValProSer
XM_011526838.1:c.2972-673_2972-665dup	XP_011525140.1:n.2972-673_2972-665dup
XM_011526839.1:c.2782_2790dup	XP_011525141.1:p.Ser930_Ser931insValProSer
XM_011526840.1:c.2125_2133dup	XP_011525142.1:p.Ser711_Ser712insValProSer
XM_011526841.1:c.1711_1719dup	XP_011525143.1:p.Ser573_Ser574insValProSer
XM_011526842.1:c.1564_1572dup	XP_011525144.1:p.Ser524_Ser525insValProSer
XM_011526843.1:c.880_888dup	XP_011525145.1:p.Ser296_Ser297insValProSer
XM_011526844.1:c.880_888dup	XP_011525146.1:p.Ser296_Ser297insValProSer
XM_011526840.2:c.2125_2133dup	XP_011525142.1:p.Ser711_Ser712insValProSer
XM_011526841.2:c.1711_1719dup	XP_011525143.1:p.Ser573_Ser574insValProSer
XM_011526844.2:c.880_888dup	XP_011525146.1:p.Ser296_Ser297insValProSer
XM_017026665.1:c.3133_3141dup	XP_016882154.1:p.Ser1047_Ser1048insValProSer
NM_001083961.2:c.3133_3141dup MANE Select	NP_001077430.1:p.Ser1047_Ser1048insValProSer
NM_173636.5:c.3133_3141dup	NP_775907.4:p.Ser1047_Ser1048insValProSer