Canonical Allele Identifier: CA632786883

Gene: WDR62

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36101765del , CM000681.2:g.36101765del	GRCh38
NC_000019.9:g.36592667del , CM000681.1:g.36592667del	GRCh37
NC_000019.8:g.41284507del	NCBI36
NG_028101.1:g.51885del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.3073del	ENSP00000270301.6:p.His1025IlefsTer?
ENST00000401500.7:c.3073del MANE Select	ENSP00000384792.1:p.His1025IlefsTer?
ENST00000587391.6:c.*2109del	ENSP00000465525.1:n.*2109del
ENST00000679357.1:c.863del
ENST00000679422.1:c.762-249del
ENST00000679682.1:c.3058del	ENSP00000506226.1:p.His1020IlefsTer?
ENST00000679714.1:c.3067del	ENSP00000506627.1:p.His1023IlefsTer?
ENST00000679757.1:c.2722del	ENSP00000505158.1:p.His908IlefsTer?
ENST00000679858.1:c.*2216del	ENSP00000505655.1:n.*2216del
ENST00000680211.1:c.-327del	ENSP00000506102.1:n.-327del
ENST00000680349.1:n.1056del
ENST00000680403.1:c.3073del	ENSP00000505677.1:p.His1025IlefsTer?
ENST00000680564.1:c.2971+448del	ENSP00000505582.1:n.2971+448del
ENST00000680590.1:c.*1468del	ENSP00000505350.1:n.*1468del
ENST00000680773.1:n.750del
ENST00000680806.1:c.*1801-249del	ENSP00000506418.1:n.*1801-249del
ENST00000680997.1:n.420del
ENST00000681088.1:c.735del
ENST00000681608.1:n.21del
ENST00000681625.1:c.*405del	ENSP00000505555.1:n.*405del
ENST00000270301.11:c.3073del	ENSP00000270301.6:p.His1025IlefsTer?
ENST00000401500.6:c.3073del	ENSP00000384792.1:p.His1025IlefsTer?
ENST00000587391.5:c.*2109del	ENSP00000465525.1:n.*2109del
NM_001083961.1:c.3073del	NP_001077430.1:p.His1025IlefsTer?
NM_173636.4:c.3073del	NP_775907.4:p.His1025IlefsTer?
XM_005258809.2:c.2972-249del	XP_005258866.1:n.2972-249del
XM_011526837.1:c.3058del	XP_011525139.1:p.His1020IlefsTer?
XM_011526838.1:c.2971+448del	XP_011525140.1:n.2971+448del
XM_011526839.1:c.2722del	XP_011525141.1:p.His908IlefsTer?
XM_011526840.1:c.2065del	XP_011525142.1:p.His689IlefsTer?
XM_011526841.1:c.1651del	XP_011525143.1:p.His551IlefsTer?
XM_011526842.1:c.1504del	XP_011525144.1:p.His502IlefsTer?
XM_011526843.1:c.820del	XP_011525145.1:p.His274IlefsTer?
XM_011526844.1:c.820del	XP_011525146.1:p.His274IlefsTer?
XM_011526840.2:c.2065del	XP_011525142.1:p.His689IlefsTer?
XM_011526841.2:c.1651del	XP_011525143.1:p.His551IlefsTer?
XM_011526844.2:c.820del	XP_011525146.1:p.His274IlefsTer?
XM_017026665.1:c.3073del	XP_016882154.1:p.His1025IlefsTer?
NM_001083961.2:c.3073del MANE Select	NP_001077430.1:p.His1025IlefsTer?
NM_173636.5:c.3073del	NP_775907.4:p.His1025IlefsTer?