Canonical Allele Identifier: CA2576761876

Gene: WDR62

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36104625_36104626insA , CM000681.2:g.36104625_36104626insA	GRCh38
NC_000019.9:g.36595527_36595528insA , CM000681.1:g.36595527_36595528insA	GRCh37
NC_000019.8:g.41287367_41287368insA	NCBI36
NG_028101.1:g.54745_54746insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.4246_4247insA	ENSP00000270301.6:p.Leu1416TyrfsTer?
ENST00000401500.7:c.4261_4262insA MANE Select	ENSP00000384792.1:p.Leu1421TyrfsTer?
ENST00000587391.6:c.*4121_*4122insA	ENSP00000465525.1:n.*4121_*4122insA
ENST00000679357.1:c.2341_2342insA
ENST00000679598.1:c.1006_1007insA
ENST00000679682.1:c.4246_4247insA	ENSP00000506226.1:p.Leu1416TyrfsTer?
ENST00000679714.1:c.4255_4256insA	ENSP00000506627.1:p.Leu1419TyrfsTer?
ENST00000679757.1:c.3910_3911insA	ENSP00000505158.1:p.Leu1304TyrfsTer?
ENST00000679858.1:c.*3643_*3644insA	ENSP00000505655.1:n.*3643_*3644insA
ENST00000680211.1:c.862_863insA	ENSP00000506102.1:p.Leu288TyrfsTer?
ENST00000680280.1:n.1764_1765insA
ENST00000680349.1:n.2910_2911insA
ENST00000680403.1:c.4246_4247insA	ENSP00000505677.1:p.Leu1416TyrfsTer?
ENST00000680564.1:c.4012_4013insA	ENSP00000505582.1:p.Leu1338TyrfsTer?
ENST00000680590.1:c.*2641_*2642insA	ENSP00000505350.1:n.*2641_*2642insA
ENST00000680597.1:c.994_995insA
ENST00000680739.1:c.1276_1277insA
ENST00000680773.1:n.2762_2763insA
ENST00000680806.1:c.*3564_*3565insA	ENSP00000506418.1:n.*3564_*3565insA
ENST00000680997.1:n.2193_2194insA
ENST00000681608.1:n.2106_2107insA
ENST00000681625.1:c.*1593_*1594insA	ENSP00000505555.1:n.*1593_*1594insA
ENST00000681648.1:n.2312_2313insA
ENST00000270301.11:c.4246_4247insA	ENSP00000270301.6:p.Leu1416TyrfsTer?
ENST00000401500.6:c.4261_4262insA	ENSP00000384792.1:p.Leu1421TyrfsTer?
ENST00000587391.5:c.*4121_*4122insA	ENSP00000465525.1:n.*4121_*4122insA
NM_001083961.1:c.4261_4262insA	NP_001077430.1:p.Leu1421TyrfsTer?
NM_173636.4:c.4246_4247insA	NP_775907.4:p.Leu1416TyrfsTer?
XM_005258809.2:c.4150_4151insA	XP_005258866.1:p.Leu1384TyrfsTer?
XM_011526837.1:c.4246_4247insA	XP_011525139.1:p.Leu1416TyrfsTer?
XM_011526838.1:c.4012_4013insA	XP_011525140.1:p.Leu1338TyrfsTer?
XM_011526839.1:c.3910_3911insA	XP_011525141.1:p.Leu1304TyrfsTer?
XM_011526840.1:c.3253_3254insA	XP_011525142.1:p.Leu1085TyrfsTer?
XM_011526841.1:c.2839_2840insA	XP_011525143.1:p.Leu947TyrfsTer?
XM_011526842.1:c.2692_2693insA	XP_011525144.1:p.Leu898TyrfsTer?
XM_011526843.1:c.2008_2009insA	XP_011525145.1:p.Leu670TyrfsTer?
XM_011526844.1:c.2008_2009insA	XP_011525146.1:p.Leu670TyrfsTer?
XM_011526840.2:c.3253_3254insA	XP_011525142.1:p.Leu1085TyrfsTer?
XM_011526841.2:c.2839_2840insA	XP_011525143.1:p.Leu947TyrfsTer?
XM_011526844.2:c.2008_2009insA	XP_011525146.1:p.Leu670TyrfsTer?
XM_017026665.1:c.4261_4262insA	XP_016882154.1:p.Leu1421TyrfsTer?
NM_001083961.2:c.4261_4262insA MANE Select	NP_001077430.1:p.Leu1421TyrfsTer?
NM_173636.5:c.4246_4247insA	NP_775907.4:p.Leu1416TyrfsTer?