Canonical Allele Identifier: CA507107597

Gene: WDR62

Linked Data

• MyVariant Identifiers: chr19:g.36593041_36593042insC (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36102144dup , CM000681.2:g.36102144dup	GRCh38
NC_000019.9:g.36593046dup , CM000681.1:g.36593046dup	GRCh37
NC_000019.8:g.41284886dup	NCBI36
NG_028101.1:g.52264dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.3213dup	ENSP00000270301.6:p.Cys1072LeufsTer11
ENST00000401500.7:c.3213dup MANE Select	ENSP00000384792.1:p.Cys1072LeufsTer16
ENST00000587391.6:c.*2488dup	ENSP00000465525.1:n.*2488dup
ENST00000679357.1:c.1003dup
ENST00000679422.1:c.892dup
ENST00000679682.1:c.3198dup	ENSP00000506226.1:p.Cys1067LeufsTer16
ENST00000679714.1:c.3207dup	ENSP00000506627.1:p.Cys1070LeufsTer16
ENST00000679757.1:c.2862dup	ENSP00000505158.1:p.Cys955LeufsTer16
ENST00000679858.1:c.*2595dup	ENSP00000505655.1:n.*2595dup
ENST00000680211.1:c.-187dup	ENSP00000506102.1:n.-187dup
ENST00000680349.1:n.1196dup
ENST00000680403.1:c.3213dup	ENSP00000505677.1:p.Cys1072LeufsTer11
ENST00000680564.1:c.2972-593dup	ENSP00000505582.1:n.2972-593dup
ENST00000680590.1:c.*1608dup	ENSP00000505350.1:n.*1608dup
ENST00000680739.1:c.131dup
ENST00000680773.1:n.1129dup
ENST00000680806.1:c.*1931dup	ENSP00000506418.1:n.*1931dup
ENST00000680997.1:n.560dup
ENST00000681088.1:c.875dup
ENST00000681608.1:n.161dup
ENST00000681625.1:c.*545dup	ENSP00000505555.1:n.*545dup
ENST00000270301.11:c.3213dup	ENSP00000270301.6:p.Cys1072LeufsTer11
ENST00000401500.6:c.3213dup	ENSP00000384792.1:p.Cys1072LeufsTer16
ENST00000587391.5:c.*2488dup	ENSP00000465525.1:n.*2488dup
NM_001083961.1:c.3213dup	NP_001077430.1:p.Cys1072LeufsTer16
NM_173636.4:c.3213dup	NP_775907.4:p.Cys1072LeufsTer11
XM_005258809.2:c.3102dup	XP_005258866.1:p.Cys1035LeufsTer16
XM_011526837.1:c.3198dup	XP_011525139.1:p.Cys1067LeufsTer16
XM_011526838.1:c.2972-593dup	XP_011525140.1:n.2972-593dup
XM_011526839.1:c.2862dup	XP_011525141.1:p.Cys955LeufsTer16
XM_011526840.1:c.2205dup	XP_011525142.1:p.Cys736LeufsTer16
XM_011526841.1:c.1791dup	XP_011525143.1:p.Cys598LeufsTer16
XM_011526842.1:c.1644dup	XP_011525144.1:p.Cys549LeufsTer16
XM_011526843.1:c.960dup	XP_011525145.1:p.Cys321LeufsTer16
XM_011526844.1:c.960dup	XP_011525146.1:p.Cys321LeufsTer16
XM_011526840.2:c.2205dup	XP_011525142.1:p.Cys736LeufsTer16
XM_011526841.2:c.1791dup	XP_011525143.1:p.Cys598LeufsTer16
XM_011526844.2:c.960dup	XP_011525146.1:p.Cys321LeufsTer16
XM_017026665.1:c.3213dup	XP_016882154.1:p.Cys1072LeufsTer16
NM_001083961.2:c.3213dup MANE Select	NP_001077430.1:p.Cys1072LeufsTer16
NM_173636.5:c.3213dup	NP_775907.4:p.Cys1072LeufsTer11