Canonical Allele Identifier: CA2584644276

Gene: WDR62

Linked Data

• gnomAD v4: 19-36101733-AC-A

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36101736del , CM000681.2:g.36101736del	GRCh38
NC_000019.9:g.36592638del , CM000681.1:g.36592638del	GRCh37
NC_000019.8:g.41284478del	NCBI36
NG_028101.1:g.51856del

Transcript Alleles

HGVS	Amino-acid change
ENST00000270301.12:c.3044del	ENSP00000270301.6:p.Pro1015LeufsTer?
ENST00000401500.7:c.3044del MANE Select	ENSP00000384792.1:p.Pro1015LeufsTer?
ENST00000587391.6:c.*2080del	ENSP00000465525.1:n.*2080del
ENST00000679357.1:c.834del
ENST00000679422.1:c.762-278del
ENST00000679682.1:c.3029del	ENSP00000506226.1:p.Pro1010LeufsTer?
ENST00000679714.1:c.3038del	ENSP00000506627.1:p.Pro1013LeufsTer?
ENST00000679757.1:c.2693del	ENSP00000505158.1:p.Pro898LeufsTer?
ENST00000679858.1:c.*2187del	ENSP00000505655.1:n.*2187del
ENST00000680211.1:c.-356del	ENSP00000506102.1:n.-356del
ENST00000680349.1:n.1027del
ENST00000680403.1:c.3044del	ENSP00000505677.1:p.Pro1015LeufsTer?
ENST00000680564.1:c.2971+419del	ENSP00000505582.1:n.2971+419del
ENST00000680590.1:c.*1439del	ENSP00000505350.1:n.*1439del
ENST00000680773.1:n.721del
ENST00000680806.1:c.*1801-278del	ENSP00000506418.1:n.*1801-278del
ENST00000680997.1:n.391del
ENST00000681088.1:c.706del
ENST00000681625.1:c.*376del	ENSP00000505555.1:n.*376del
ENST00000270301.11:c.3044del	ENSP00000270301.6:p.Pro1015LeufsTer?
ENST00000401500.6:c.3044del	ENSP00000384792.1:p.Pro1015LeufsTer?
ENST00000587391.5:c.*2080del	ENSP00000465525.1:n.*2080del
NM_001083961.1:c.3044del	NP_001077430.1:p.Pro1015LeufsTer?
NM_173636.4:c.3044del	NP_775907.4:p.Pro1015LeufsTer?
XM_005258809.2:c.2972-278del	XP_005258866.1:n.2972-278del
XM_011526837.1:c.3029del	XP_011525139.1:p.Pro1010LeufsTer?
XM_011526838.1:c.2971+419del	XP_011525140.1:n.2971+419del
XM_011526839.1:c.2693del	XP_011525141.1:p.Pro898LeufsTer?
XM_011526840.1:c.2036del	XP_011525142.1:p.Pro679LeufsTer?
XM_011526841.1:c.1622del	XP_011525143.1:p.Pro541LeufsTer?
XM_011526842.1:c.1475del	XP_011525144.1:p.Pro492LeufsTer?
XM_011526843.1:c.791del	XP_011525145.1:p.Pro264LeufsTer?
XM_011526844.1:c.791del	XP_011525146.1:p.Pro264LeufsTer?
XM_011526840.2:c.2036del	XP_011525142.1:p.Pro679LeufsTer?
XM_011526841.2:c.1622del	XP_011525143.1:p.Pro541LeufsTer?
XM_011526844.2:c.791del	XP_011525146.1:p.Pro264LeufsTer?
XM_017026665.1:c.3044del	XP_016882154.1:p.Pro1015LeufsTer?
NM_001083961.2:c.3044del MANE Select	NP_001077430.1:p.Pro1015LeufsTer?
NM_173636.5:c.3044del	NP_775907.4:p.Pro1015LeufsTer?