Canonical Allele Identifier: CA2333972224

Gene: WDR62

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36104627_36104629delinsGCA , CM000681.2:g.36104627_36104629delinsGCA	GRCh38
NC_000019.9:g.36595529_36595531delinsGCA , CM000681.1:g.36595529_36595531delinsGCA	GRCh37
NC_000019.8:g.41287369_41287371delinsGCA	NCBI36
NG_028101.1:g.54747_54749delinsGCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.4248_4250delinsGCA	ENSP00000270301.6:p.Leu1416=
ENST00000401500.7:c.4263_4265delinsGCA MANE Select	ENSP00000384792.1:p.Leu1421=
ENST00000587391.6:c.*4123_*4125delinsGCA	ENSP00000465525.1:n.*4123_*4125delinsGCA
ENST00000679357.1:c.2343_2345delinsGCA
ENST00000679598.1:c.1008_1010delinsGCA
ENST00000679682.1:c.4248_4250delinsGCA	ENSP00000506226.1:p.Leu1416=
ENST00000679714.1:c.4257_4259delinsGCA	ENSP00000506627.1:p.Leu1419=
ENST00000679757.1:c.3912_3914delinsGCA	ENSP00000505158.1:p.Leu1304=
ENST00000679858.1:c.*3645_*3647delinsGCA	ENSP00000505655.1:n.*3645_*3647delinsGCA
ENST00000680211.1:c.864_866delinsGCA	ENSP00000506102.1:p.Leu288=
ENST00000680280.1:n.1766_1768delinsGCA
ENST00000680349.1:n.2912_2914delinsGCA
ENST00000680403.1:c.4248_4250delinsGCA	ENSP00000505677.1:p.Leu1416=
ENST00000680564.1:c.4014_4016delinsGCA	ENSP00000505582.1:p.Leu1338=
ENST00000680590.1:c.*2643_*2645delinsGCA	ENSP00000505350.1:n.*2643_*2645delinsGCA
ENST00000680597.1:c.996_998delinsGCA
ENST00000680739.1:c.1278_1280delinsGCA
ENST00000680773.1:n.2764_2766delinsGCA
ENST00000680806.1:c.*3566_*3568delinsGCA	ENSP00000506418.1:n.*3566_*3568delinsGCA
ENST00000680997.1:n.2195_2197delinsGCA
ENST00000681608.1:n.2108_2110delinsGCA
ENST00000681625.1:c.*1595_*1597delinsGCA	ENSP00000505555.1:n.*1595_*1597delinsGCA
ENST00000681648.1:n.2314_2316delinsGCA
ENST00000270301.11:c.4248_4250delinsGCA	ENSP00000270301.6:p.Leu1416=
ENST00000401500.6:c.4263_4265delinsGCA	ENSP00000384792.1:p.Leu1421=
ENST00000587391.5:c.*4123_*4125delinsGCA	ENSP00000465525.1:n.*4123_*4125delinsGCA
NM_001083961.1:c.4263_4265delinsGCA	NP_001077430.1:p.Leu1421=
NM_173636.4:c.4248_4250delinsGCA	NP_775907.4:p.Leu1416=
XM_005258809.2:c.4152_4154delinsGCA	XP_005258866.1:p.Leu1384=
XM_011526837.1:c.4248_4250delinsGCA	XP_011525139.1:p.Leu1416=
XM_011526838.1:c.4014_4016delinsGCA	XP_011525140.1:p.Leu1338=
XM_011526839.1:c.3912_3914delinsGCA	XP_011525141.1:p.Leu1304=
XM_011526840.1:c.3255_3257delinsGCA	XP_011525142.1:p.Leu1085=
XM_011526841.1:c.2841_2843delinsGCA	XP_011525143.1:p.Leu947=
XM_011526842.1:c.2694_2696delinsGCA	XP_011525144.1:p.Leu898=
XM_011526843.1:c.2010_2012delinsGCA	XP_011525145.1:p.Leu670=
XM_011526844.1:c.2010_2012delinsGCA	XP_011525146.1:p.Leu670=
XM_011526840.2:c.3255_3257delinsGCA	XP_011525142.1:p.Leu1085=
XM_011526841.2:c.2841_2843delinsGCA	XP_011525143.1:p.Leu947=
XM_011526844.2:c.2010_2012delinsGCA	XP_011525146.1:p.Leu670=
XM_017026665.1:c.4263_4265delinsGCA	XP_016882154.1:p.Leu1421=
NM_001083961.2:c.4263_4265delinsGCA MANE Select	NP_001077430.1:p.Leu1421=
NM_173636.5:c.4248_4250delinsGCA	NP_775907.4:p.Leu1416=