Canonical Allele Identifier: CA2333972213

Gene: WDR62

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36104609_36104613delinsCAGGG , CM000681.2:g.36104609_36104613delinsCAGGG	GRCh38
NC_000019.9:g.36595511_36595515delinsCAGGG , CM000681.1:g.36595511_36595515delinsCAGGG	GRCh37
NC_000019.8:g.41287351_41287355delinsCAGGG	NCBI36
NG_028101.1:g.54729_54733delinsCAGGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.4230_4234delinsCAGGG	ENSP00000270301.6:p.Ser1410=
ENST00000401500.7:c.4245_4249delinsCAGGG MANE Select	ENSP00000384792.1:p.Ser1415=
ENST00000587391.6:c.*4105_*4109delinsCAGGG	ENSP00000465525.1:n.*4105_*4109delinsCAGGG
ENST00000679357.1:c.2325_2329delinsCAGGG
ENST00000679598.1:c.990_994delinsCAGGG
ENST00000679682.1:c.4230_4234delinsCAGGG	ENSP00000506226.1:p.Ser1410=
ENST00000679714.1:c.4239_4243delinsCAGGG	ENSP00000506627.1:p.Ser1413=
ENST00000679757.1:c.3894_3898delinsCAGGG	ENSP00000505158.1:p.Ser1298=
ENST00000679858.1:c.*3627_*3631delinsCAGGG	ENSP00000505655.1:n.*3627_*3631delinsCAGGG
ENST00000680211.1:c.846_850delinsCAGGG	ENSP00000506102.1:p.Ser282=
ENST00000680280.1:n.1748_1752delinsCAGGG
ENST00000680349.1:n.2894_2898delinsCAGGG
ENST00000680403.1:c.4230_4234delinsCAGGG	ENSP00000505677.1:p.Ser1410=
ENST00000680564.1:c.3996_4000delinsCAGGG	ENSP00000505582.1:p.Ser1332=
ENST00000680590.1:c.*2625_*2629delinsCAGGG	ENSP00000505350.1:n.*2625_*2629delinsCAGGG
ENST00000680597.1:c.978_982delinsCAGGG
ENST00000680739.1:c.1260_1264delinsCAGGG
ENST00000680773.1:n.2746_2750delinsCAGGG
ENST00000680806.1:c.*3548_*3552delinsCAGGG	ENSP00000506418.1:n.*3548_*3552delinsCAGGG
ENST00000680997.1:n.2177_2181delinsCAGGG
ENST00000681608.1:n.2090_2094delinsCAGGG
ENST00000681625.1:c.*1577_*1581delinsCAGGG	ENSP00000505555.1:n.*1577_*1581delinsCAGGG
ENST00000681648.1:n.2296_2300delinsCAGGG
ENST00000270301.11:c.4230_4234delinsCAGGG	ENSP00000270301.6:p.Ser1410=
ENST00000401500.6:c.4245_4249delinsCAGGG	ENSP00000384792.1:p.Ser1415=
ENST00000587391.5:c.*4105_*4109delinsCAGGG	ENSP00000465525.1:n.*4105_*4109delinsCAGGG
NM_001083961.1:c.4245_4249delinsCAGGG	NP_001077430.1:p.Ser1415=
NM_173636.4:c.4230_4234delinsCAGGG	NP_775907.4:p.Ser1410=
XM_005258809.2:c.4134_4138delinsCAGGG	XP_005258866.1:p.Ser1378=
XM_011526837.1:c.4230_4234delinsCAGGG	XP_011525139.1:p.Ser1410=
XM_011526838.1:c.3996_4000delinsCAGGG	XP_011525140.1:p.Ser1332=
XM_011526839.1:c.3894_3898delinsCAGGG	XP_011525141.1:p.Ser1298=
XM_011526840.1:c.3237_3241delinsCAGGG	XP_011525142.1:p.Ser1079=
XM_011526841.1:c.2823_2827delinsCAGGG	XP_011525143.1:p.Ser941=
XM_011526842.1:c.2676_2680delinsCAGGG	XP_011525144.1:p.Ser892=
XM_011526843.1:c.1992_1996delinsCAGGG	XP_011525145.1:p.Ser664=
XM_011526844.1:c.1992_1996delinsCAGGG	XP_011525146.1:p.Ser664=
XM_011526840.2:c.3237_3241delinsCAGGG	XP_011525142.1:p.Ser1079=
XM_011526841.2:c.2823_2827delinsCAGGG	XP_011525143.1:p.Ser941=
XM_011526844.2:c.1992_1996delinsCAGGG	XP_011525146.1:p.Ser664=
XM_017026665.1:c.4245_4249delinsCAGGG	XP_016882154.1:p.Ser1415=
NM_001083961.2:c.4245_4249delinsCAGGG MANE Select	NP_001077430.1:p.Ser1415=
NM_173636.5:c.4230_4234delinsCAGGG	NP_775907.4:p.Ser1410=