Canonical Allele Identifier: CA2333972193

Gene: WDR62

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36104568_36104572delinsGTGCC , CM000681.2:g.36104568_36104572delinsGTGCC	GRCh38
NC_000019.9:g.36595470_36595474delinsGTGCC , CM000681.1:g.36595470_36595474delinsGTGCC	GRCh37
NC_000019.8:g.41287310_41287314delinsGTGCC	NCBI36
NG_028101.1:g.54688_54692delinsGTGCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.4189_4193delinsGTGCC	ENSP00000270301.6:p.Val1397=
ENST00000401500.7:c.4204_4208delinsGTGCC MANE Select	ENSP00000384792.1:p.Val1402=
ENST00000587391.6:c.*4064_*4068delinsGTGCC	ENSP00000465525.1:n.*4064_*4068delinsGTGCC
ENST00000679357.1:c.2284_2288delinsGTGCC
ENST00000679598.1:c.949_953delinsGTGCC
ENST00000679682.1:c.4189_4193delinsGTGCC	ENSP00000506226.1:p.Val1397=
ENST00000679714.1:c.4198_4202delinsGTGCC	ENSP00000506627.1:p.Val1400=
ENST00000679757.1:c.3853_3857delinsGTGCC	ENSP00000505158.1:p.Val1285=
ENST00000679858.1:c.*3586_*3590delinsGTGCC	ENSP00000505655.1:n.*3586_*3590delinsGTGCC
ENST00000680211.1:c.805_809delinsGTGCC	ENSP00000506102.1:p.Val269=
ENST00000680280.1:n.1707_1711delinsGTGCC
ENST00000680349.1:n.2853_2857delinsGTGCC
ENST00000680403.1:c.4189_4193delinsGTGCC	ENSP00000505677.1:p.Val1397=
ENST00000680564.1:c.3955_3959delinsGTGCC	ENSP00000505582.1:p.Val1319=
ENST00000680590.1:c.*2584_*2588delinsGTGCC	ENSP00000505350.1:n.*2584_*2588delinsGTGCC
ENST00000680597.1:c.937_941delinsGTGCC
ENST00000680739.1:c.1219_1223delinsGTGCC
ENST00000680773.1:n.2705_2709delinsGTGCC
ENST00000680806.1:c.*3507_*3511delinsGTGCC	ENSP00000506418.1:n.*3507_*3511delinsGTGCC
ENST00000680997.1:n.2136_2140delinsGTGCC
ENST00000681608.1:n.2049_2053delinsGTGCC
ENST00000681625.1:c.*1536_*1540delinsGTGCC	ENSP00000505555.1:n.*1536_*1540delinsGTGCC
ENST00000681648.1:n.2255_2259delinsGTGCC
ENST00000270301.11:c.4189_4193delinsGTGCC	ENSP00000270301.6:p.Val1397=
ENST00000401500.6:c.4204_4208delinsGTGCC	ENSP00000384792.1:p.Val1402=
ENST00000587391.5:c.*4064_*4068delinsGTGCC	ENSP00000465525.1:n.*4064_*4068delinsGTGCC
NM_001083961.1:c.4204_4208delinsGTGCC	NP_001077430.1:p.Val1402=
NM_173636.4:c.4189_4193delinsGTGCC	NP_775907.4:p.Val1397=
XM_005258809.2:c.4093_4097delinsGTGCC	XP_005258866.1:p.Val1365=
XM_011526837.1:c.4189_4193delinsGTGCC	XP_011525139.1:p.Val1397=
XM_011526838.1:c.3955_3959delinsGTGCC	XP_011525140.1:p.Val1319=
XM_011526839.1:c.3853_3857delinsGTGCC	XP_011525141.1:p.Val1285=
XM_011526840.1:c.3196_3200delinsGTGCC	XP_011525142.1:p.Val1066=
XM_011526841.1:c.2782_2786delinsGTGCC	XP_011525143.1:p.Val928=
XM_011526842.1:c.2635_2639delinsGTGCC	XP_011525144.1:p.Val879=
XM_011526843.1:c.1951_1955delinsGTGCC	XP_011525145.1:p.Val651=
XM_011526844.1:c.1951_1955delinsGTGCC	XP_011525146.1:p.Val651=
XM_011526840.2:c.3196_3200delinsGTGCC	XP_011525142.1:p.Val1066=
XM_011526841.2:c.2782_2786delinsGTGCC	XP_011525143.1:p.Val928=
XM_011526844.2:c.1951_1955delinsGTGCC	XP_011525146.1:p.Val651=
XM_017026665.1:c.4204_4208delinsGTGCC	XP_016882154.1:p.Val1402=
NM_001083961.2:c.4204_4208delinsGTGCC MANE Select	NP_001077430.1:p.Val1402=
NM_173636.5:c.4189_4193delinsGTGCC	NP_775907.4:p.Val1397=