Canonical Allele Identifier: CA632787290

Gene: WDR62

Linked Data

• dbSNP Id: rs1233064752
• gnomAD v2: 19-36592870-ACT-A
• gnomAD v4: 19-36101968-ACT-A
• MyVariant Identifiers: chr19:g.36592871_36592872del (hg19) ; chr19:g.36101969_36101970del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36101970_36101971del , CM000681.2:g.36101970_36101971del	GRCh38
NC_000019.9:g.36592872_36592873del , CM000681.1:g.36592872_36592873del	GRCh37
NC_000019.8:g.41284712_41284713del	NCBI36
NG_028101.1:g.52090_52091del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.3083-44_3083-43del	ENSP00000270301.6:n.3083-44_3083-43del
ENST00000401500.7:c.3083-44_3083-43del MANE Select	ENSP00000384792.1:n.3083-44_3083-43del
ENST00000587391.6:c.*2314_*2315del	ENSP00000465525.1:n.*2314_*2315del
ENST00000679357.1:c.873-44_873-43del
ENST00000679422.1:c.762-44_762-43del
ENST00000679682.1:c.3068-44_3068-43del	ENSP00000506226.1:n.3068-44_3068-43del
ENST00000679714.1:c.3077-44_3077-43del	ENSP00000506627.1:n.3077-44_3077-43del
ENST00000679757.1:c.2732-44_2732-43del	ENSP00000505158.1:n.2732-44_2732-43del
ENST00000679858.1:c.*2421_*2422del	ENSP00000505655.1:n.*2421_*2422del
ENST00000680211.1:c.-317-44_-317-43del	ENSP00000506102.1:n.-317-44_-317-43del
ENST00000680349.1:n.1066-44_1066-43del
ENST00000680403.1:c.3083-44_3083-43del	ENSP00000505677.1:n.3083-44_3083-43del
ENST00000680564.1:c.2971+653_2971+654del	ENSP00000505582.1:n.2971+653_2971+654del
ENST00000680590.1:c.*1478-44_*1478-43del	ENSP00000505350.1:n.*1478-44_*1478-43del
ENST00000680773.1:n.955_956del
ENST00000680806.1:c.*1801-44_*1801-43del	ENSP00000506418.1:n.*1801-44_*1801-43del
ENST00000680997.1:n.430-44_430-43del
ENST00000681088.1:c.745-44_745-43del
ENST00000681608.1:n.31-44_31-43del
ENST00000681625.1:c.*415-44_*415-43del	ENSP00000505555.1:n.*415-44_*415-43del
ENST00000270301.11:c.3083-44_3083-43del	ENSP00000270301.6:n.3083-44_3083-43del
ENST00000401500.6:c.3083-44_3083-43del	ENSP00000384792.1:n.3083-44_3083-43del
ENST00000587391.5:c.*2314_*2315del	ENSP00000465525.1:n.*2314_*2315del
NM_001083961.1:c.3083-44_3083-43del	NP_001077430.1:n.3083-44_3083-43del
NM_173636.4:c.3083-44_3083-43del	NP_775907.4:n.3083-44_3083-43del
XM_005258809.2:c.2972-44_2972-43del	XP_005258866.1:n.2972-44_2972-43del
XM_011526837.1:c.3068-44_3068-43del	XP_011525139.1:n.3068-44_3068-43del
XM_011526838.1:c.2971+653_2971+654del	XP_011525140.1:n.2971+653_2971+654del
XM_011526839.1:c.2732-44_2732-43del	XP_011525141.1:n.2732-44_2732-43del
XM_011526840.1:c.2075-44_2075-43del	XP_011525142.1:n.2075-44_2075-43del
XM_011526841.1:c.1661-44_1661-43del	XP_011525143.1:n.1661-44_1661-43del
XM_011526842.1:c.1514-44_1514-43del	XP_011525144.1:n.1514-44_1514-43del
XM_011526843.1:c.830-44_830-43del	XP_011525145.1:n.830-44_830-43del
XM_011526844.1:c.830-44_830-43del	XP_011525146.1:n.830-44_830-43del
XM_011526840.2:c.2075-44_2075-43del	XP_011525142.1:n.2075-44_2075-43del
XM_011526841.2:c.1661-44_1661-43del	XP_011525143.1:n.1661-44_1661-43del
XM_011526844.2:c.830-44_830-43del	XP_011525146.1:n.830-44_830-43del
XM_017026665.1:c.3083-44_3083-43del	XP_016882154.1:n.3083-44_3083-43del
NM_001083961.2:c.3083-44_3083-43del MANE Select	NP_001077430.1:n.3083-44_3083-43del
NM_173636.5:c.3083-44_3083-43del	NP_775907.4:n.3083-44_3083-43del