Canonical Allele Identifier: CA2333970905

Gene: WDR62

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36102029_36102032delinsCAGA , CM000681.2:g.36102029_36102032delinsCAGA	GRCh38
NC_000019.9:g.36592931_36592934delinsCAGA , CM000681.1:g.36592931_36592934delinsCAGA	GRCh37
NC_000019.8:g.41284771_41284774delinsCAGA	NCBI36
NG_028101.1:g.52149_52152delinsCAGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.3098_3101delinsCAGA	ENSP00000270301.6:p.Thr1033=
ENST00000401500.7:c.3098_3101delinsCAGA MANE Select	ENSP00000384792.1:p.Thr1033=
ENST00000587391.6:c.*2373_*2376delinsCAGA	ENSP00000465525.1:n.*2373_*2376delinsCAGA
ENST00000679357.1:c.888_891delinsCAGA
ENST00000679422.1:c.777_780delinsCAGA
ENST00000679682.1:c.3083_3086delinsCAGA	ENSP00000506226.1:p.Thr1028=
ENST00000679714.1:c.3092_3095delinsCAGA	ENSP00000506627.1:p.Thr1031=
ENST00000679757.1:c.2747_2750delinsCAGA	ENSP00000505158.1:p.Thr916=
ENST00000679858.1:c.*2480_*2483delinsCAGA	ENSP00000505655.1:n.*2480_*2483delinsCAGA
ENST00000680211.1:c.-302_-299delinsCAGA	ENSP00000506102.1:n.-302_-299delinsCAGA
ENST00000680349.1:n.1081_1084delinsCAGA
ENST00000680403.1:c.3098_3101delinsCAGA	ENSP00000505677.1:p.Thr1033=
ENST00000680564.1:c.2972-708_2972-705delinsCAGA	ENSP00000505582.1:n.2972-708_2972-705delinsCAGA
ENST00000680590.1:c.*1493_*1496delinsCAGA	ENSP00000505350.1:n.*1493_*1496delinsCAGA
ENST00000680739.1:c.16_19delinsCAGA
ENST00000680773.1:n.1014_1017delinsCAGA
ENST00000680806.1:c.*1816_*1819delinsCAGA	ENSP00000506418.1:n.*1816_*1819delinsCAGA
ENST00000680997.1:n.445_448delinsCAGA
ENST00000681088.1:c.760_763delinsCAGA
ENST00000681608.1:n.46_49delinsCAGA
ENST00000681625.1:c.*430_*433delinsCAGA	ENSP00000505555.1:n.*430_*433delinsCAGA
ENST00000270301.11:c.3098_3101delinsCAGA	ENSP00000270301.6:p.Thr1033=
ENST00000401500.6:c.3098_3101delinsCAGA	ENSP00000384792.1:p.Thr1033=
ENST00000587391.5:c.*2373_*2376delinsCAGA	ENSP00000465525.1:n.*2373_*2376delinsCAGA
NM_001083961.1:c.3098_3101delinsCAGA	NP_001077430.1:p.Thr1033=
NM_173636.4:c.3098_3101delinsCAGA	NP_775907.4:p.Thr1033=
XM_005258809.2:c.2987_2990delinsCAGA	XP_005258866.1:p.Thr996=
XM_011526837.1:c.3083_3086delinsCAGA	XP_011525139.1:p.Thr1028=
XM_011526838.1:c.2972-708_2972-705delinsCAGA	XP_011525140.1:n.2972-708_2972-705delinsCAGA
XM_011526839.1:c.2747_2750delinsCAGA	XP_011525141.1:p.Thr916=
XM_011526840.1:c.2090_2093delinsCAGA	XP_011525142.1:p.Thr697=
XM_011526841.1:c.1676_1679delinsCAGA	XP_011525143.1:p.Thr559=
XM_011526842.1:c.1529_1532delinsCAGA	XP_011525144.1:p.Thr510=
XM_011526843.1:c.845_848delinsCAGA	XP_011525145.1:p.Thr282=
XM_011526844.1:c.845_848delinsCAGA	XP_011525146.1:p.Thr282=
XM_011526840.2:c.2090_2093delinsCAGA	XP_011525142.1:p.Thr697=
XM_011526841.2:c.1676_1679delinsCAGA	XP_011525143.1:p.Thr559=
XM_011526844.2:c.845_848delinsCAGA	XP_011525146.1:p.Thr282=
XM_017026665.1:c.3098_3101delinsCAGA	XP_016882154.1:p.Thr1033=
NM_001083961.2:c.3098_3101delinsCAGA MANE Select	NP_001077430.1:p.Thr1033=
NM_173636.5:c.3098_3101delinsCAGA	NP_775907.4:p.Thr1033=