Canonical Allele Identifier: CA2333970955

Gene: WDR62

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36102128_36102132delinsCACTG , CM000681.2:g.36102128_36102132delinsCACTG	GRCh38
NC_000019.9:g.36593030_36593034delinsCACTG , CM000681.1:g.36593030_36593034delinsCACTG	GRCh37
NC_000019.8:g.41284870_41284874delinsCACTG	NCBI36
NG_028101.1:g.52248_52252delinsCACTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.3197_3201delinsCACTG	ENSP00000270301.6:p.Thr1066=
ENST00000401500.7:c.3197_3201delinsCACTG MANE Select	ENSP00000384792.1:p.Thr1066=
ENST00000587391.6:c.*2472_*2476delinsCACTG	ENSP00000465525.1:n.*2472_*2476delinsCACTG
ENST00000679357.1:c.987_991delinsCACTG
ENST00000679422.1:c.876_880delinsCACTG
ENST00000679682.1:c.3182_3186delinsCACTG	ENSP00000506226.1:p.Thr1061=
ENST00000679714.1:c.3191_3195delinsCACTG	ENSP00000506627.1:p.Thr1064=
ENST00000679757.1:c.2846_2850delinsCACTG	ENSP00000505158.1:p.Thr949=
ENST00000679858.1:c.*2579_*2583delinsCACTG	ENSP00000505655.1:n.*2579_*2583delinsCACTG
ENST00000680211.1:c.-203_-199delinsCACTG	ENSP00000506102.1:n.-203_-199delinsCACTG
ENST00000680349.1:n.1180_1184delinsCACTG
ENST00000680403.1:c.3197_3201delinsCACTG	ENSP00000505677.1:p.Thr1066=
ENST00000680564.1:c.2972-609_2972-605delinsCACTG	ENSP00000505582.1:n.2972-609_2972-605delinsCACTG
ENST00000680590.1:c.*1592_*1596delinsCACTG	ENSP00000505350.1:n.*1592_*1596delinsCACTG
ENST00000680739.1:c.115_119delinsCACTG
ENST00000680773.1:n.1113_1117delinsCACTG
ENST00000680806.1:c.*1915_*1919delinsCACTG	ENSP00000506418.1:n.*1915_*1919delinsCACTG
ENST00000680997.1:n.544_548delinsCACTG
ENST00000681088.1:c.859_863delinsCACTG
ENST00000681608.1:n.145_149delinsCACTG
ENST00000681625.1:c.*529_*533delinsCACTG	ENSP00000505555.1:n.*529_*533delinsCACTG
ENST00000270301.11:c.3197_3201delinsCACTG	ENSP00000270301.6:p.Thr1066=
ENST00000401500.6:c.3197_3201delinsCACTG	ENSP00000384792.1:p.Thr1066=
ENST00000587391.5:c.*2472_*2476delinsCACTG	ENSP00000465525.1:n.*2472_*2476delinsCACTG
NM_001083961.1:c.3197_3201delinsCACTG	NP_001077430.1:p.Thr1066=
NM_173636.4:c.3197_3201delinsCACTG	NP_775907.4:p.Thr1066=
XM_005258809.2:c.3086_3090delinsCACTG	XP_005258866.1:p.Thr1029=
XM_011526837.1:c.3182_3186delinsCACTG	XP_011525139.1:p.Thr1061=
XM_011526838.1:c.2972-609_2972-605delinsCACTG	XP_011525140.1:n.2972-609_2972-605delinsCACTG
XM_011526839.1:c.2846_2850delinsCACTG	XP_011525141.1:p.Thr949=
XM_011526840.1:c.2189_2193delinsCACTG	XP_011525142.1:p.Thr730=
XM_011526841.1:c.1775_1779delinsCACTG	XP_011525143.1:p.Thr592=
XM_011526842.1:c.1628_1632delinsCACTG	XP_011525144.1:p.Thr543=
XM_011526843.1:c.944_948delinsCACTG	XP_011525145.1:p.Thr315=
XM_011526844.1:c.944_948delinsCACTG	XP_011525146.1:p.Thr315=
XM_011526840.2:c.2189_2193delinsCACTG	XP_011525142.1:p.Thr730=
XM_011526841.2:c.1775_1779delinsCACTG	XP_011525143.1:p.Thr592=
XM_011526844.2:c.944_948delinsCACTG	XP_011525146.1:p.Thr315=
XM_017026665.1:c.3197_3201delinsCACTG	XP_016882154.1:p.Thr1066=
NM_001083961.2:c.3197_3201delinsCACTG MANE Select	NP_001077430.1:p.Thr1066=
NM_173636.5:c.3197_3201delinsCACTG	NP_775907.4:p.Thr1066=