Canonical Allele Identifier: CA2584645216

Gene: WDR62

Linked Data

• gnomAD v4: 19-36104554-GGAGT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36104558_36104561del , CM000681.2:g.36104558_36104561del	GRCh38
NC_000019.9:g.36595460_36595463del , CM000681.1:g.36595460_36595463del	GRCh37
NC_000019.8:g.41287300_41287303del	NCBI36
NG_028101.1:g.54678_54681del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.4179_4182del	ENSP00000270301.6:p.Glu1394ProfsTer15
ENST00000401500.7:c.4194_4197del MANE Select	ENSP00000384792.1:p.Glu1399ProfsTer15
ENST00000587391.6:c.*4054_*4057del	ENSP00000465525.1:n.*4054_*4057del
ENST00000679357.1:c.2274_2277del
ENST00000679598.1:c.939_942del
ENST00000679682.1:c.4179_4182del	ENSP00000506226.1:p.Glu1394ProfsTer15
ENST00000679714.1:c.4188_4191del	ENSP00000506627.1:p.Glu1397ProfsTer15
ENST00000679757.1:c.3843_3846del	ENSP00000505158.1:p.Glu1282ProfsTer15
ENST00000679858.1:c.*3576_*3579del	ENSP00000505655.1:n.*3576_*3579del
ENST00000680211.1:c.795_798del	ENSP00000506102.1:p.Glu266ProfsTer15
ENST00000680280.1:n.1697_1700del
ENST00000680349.1:n.2843_2846del
ENST00000680403.1:c.4179_4182del	ENSP00000505677.1:p.Glu1394ProfsTer15
ENST00000680564.1:c.3945_3948del	ENSP00000505582.1:p.Glu1316ProfsTer15
ENST00000680590.1:c.*2574_*2577del	ENSP00000505350.1:n.*2574_*2577del
ENST00000680597.1:c.927_930del
ENST00000680739.1:c.1209_1212del
ENST00000680773.1:n.2695_2698del
ENST00000680806.1:c.*3497_*3500del	ENSP00000506418.1:n.*3497_*3500del
ENST00000680997.1:n.2126_2129del
ENST00000681608.1:n.2039_2042del
ENST00000681625.1:c.*1526_*1529del	ENSP00000505555.1:n.*1526_*1529del
ENST00000681648.1:n.2245_2248del
ENST00000270301.11:c.4179_4182del	ENSP00000270301.6:p.Glu1394ProfsTer15
ENST00000401500.6:c.4194_4197del	ENSP00000384792.1:p.Glu1399ProfsTer15
ENST00000587391.5:c.*4054_*4057del	ENSP00000465525.1:n.*4054_*4057del
NM_001083961.1:c.4194_4197del	NP_001077430.1:p.Glu1399ProfsTer15
NM_173636.4:c.4179_4182del	NP_775907.4:p.Glu1394ProfsTer15
XM_005258809.2:c.4083_4086del	XP_005258866.1:p.Glu1362ProfsTer15
XM_011526837.1:c.4179_4182del	XP_011525139.1:p.Glu1394ProfsTer15
XM_011526838.1:c.3945_3948del	XP_011525140.1:p.Glu1316ProfsTer15
XM_011526839.1:c.3843_3846del	XP_011525141.1:p.Glu1282ProfsTer15
XM_011526840.1:c.3186_3189del	XP_011525142.1:p.Glu1063ProfsTer15
XM_011526841.1:c.2772_2775del	XP_011525143.1:p.Glu925ProfsTer15
XM_011526842.1:c.2625_2628del	XP_011525144.1:p.Glu876ProfsTer15
XM_011526843.1:c.1941_1944del	XP_011525145.1:p.Glu648ProfsTer15
XM_011526844.1:c.1941_1944del	XP_011525146.1:p.Glu648ProfsTer15
XM_011526840.2:c.3186_3189del	XP_011525142.1:p.Glu1063ProfsTer15
XM_011526841.2:c.2772_2775del	XP_011525143.1:p.Glu925ProfsTer15
XM_011526844.2:c.1941_1944del	XP_011525146.1:p.Glu648ProfsTer15
XM_017026665.1:c.4194_4197del	XP_016882154.1:p.Glu1399ProfsTer15
NM_001083961.2:c.4194_4197del MANE Select	NP_001077430.1:p.Glu1399ProfsTer15
NM_173636.5:c.4179_4182del	NP_775907.4:p.Glu1394ProfsTer15