Canonical Allele Identifier: CA2584644439

Gene: WDR62

Linked Data

• gnomAD v4: 19-36102072-C-CA

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36102073dup , CM000681.2:g.36102073dup	GRCh38
NC_000019.9:g.36592975dup , CM000681.1:g.36592975dup	GRCh37
NC_000019.8:g.41284815dup	NCBI36
NG_028101.1:g.52193dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.3142dup	ENSP00000270301.6:p.Ser1048LysfsTer18
ENST00000401500.7:c.3142dup MANE Select	ENSP00000384792.1:p.Ser1048LysfsTer18
ENST00000587391.6:c.*2417dup	ENSP00000465525.1:n.*2417dup
ENST00000679357.1:c.932dup
ENST00000679422.1:c.821dup
ENST00000679682.1:c.3127dup	ENSP00000506226.1:p.Ser1043LysfsTer18
ENST00000679714.1:c.3136dup	ENSP00000506627.1:p.Ser1046LysfsTer18
ENST00000679757.1:c.2791dup	ENSP00000505158.1:p.Ser931LysfsTer18
ENST00000679858.1:c.*2524dup	ENSP00000505655.1:n.*2524dup
ENST00000680211.1:c.-258dup	ENSP00000506102.1:n.-258dup
ENST00000680349.1:n.1125dup
ENST00000680403.1:c.3142dup	ENSP00000505677.1:p.Ser1048LysfsTer18
ENST00000680564.1:c.2972-664dup	ENSP00000505582.1:n.2972-664dup
ENST00000680590.1:c.*1537dup	ENSP00000505350.1:n.*1537dup
ENST00000680739.1:c.60dup
ENST00000680773.1:n.1058dup
ENST00000680806.1:c.*1860dup	ENSP00000506418.1:n.*1860dup
ENST00000680997.1:n.489dup
ENST00000681088.1:c.804dup
ENST00000681608.1:n.90dup
ENST00000681625.1:c.*474dup	ENSP00000505555.1:n.*474dup
ENST00000270301.11:c.3142dup	ENSP00000270301.6:p.Ser1048LysfsTer18
ENST00000401500.6:c.3142dup	ENSP00000384792.1:p.Ser1048LysfsTer18
ENST00000587391.5:c.*2417dup	ENSP00000465525.1:n.*2417dup
NM_001083961.1:c.3142dup	NP_001077430.1:p.Ser1048LysfsTer18
NM_173636.4:c.3142dup	NP_775907.4:p.Ser1048LysfsTer18
XM_005258809.2:c.3031dup	XP_005258866.1:p.Ser1011LysfsTer18
XM_011526837.1:c.3127dup	XP_011525139.1:p.Ser1043LysfsTer18
XM_011526838.1:c.2972-664dup	XP_011525140.1:n.2972-664dup
XM_011526839.1:c.2791dup	XP_011525141.1:p.Ser931LysfsTer18
XM_011526840.1:c.2134dup	XP_011525142.1:p.Ser712LysfsTer18
XM_011526841.1:c.1720dup	XP_011525143.1:p.Ser574LysfsTer18
XM_011526842.1:c.1573dup	XP_011525144.1:p.Ser525LysfsTer18
XM_011526843.1:c.889dup	XP_011525145.1:p.Ser297LysfsTer18
XM_011526844.1:c.889dup	XP_011525146.1:p.Ser297LysfsTer18
XM_011526840.2:c.2134dup	XP_011525142.1:p.Ser712LysfsTer18
XM_011526841.2:c.1720dup	XP_011525143.1:p.Ser574LysfsTer18
XM_011526844.2:c.889dup	XP_011525146.1:p.Ser297LysfsTer18
XM_017026665.1:c.3142dup	XP_016882154.1:p.Ser1048LysfsTer18
NM_001083961.2:c.3142dup MANE Select	NP_001077430.1:p.Ser1048LysfsTer18
NM_173636.5:c.3142dup	NP_775907.4:p.Ser1048LysfsTer18