Canonical Allele Identifier: CA2052905090

Gene: CEP290

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.88083863_88083867delinsAATTT , CM000674.2:g.88083863_88083867delinsAATTT	GRCh38
NC_000012.11:g.88477640_88477644delinsAATTT , CM000674.1:g.88477640_88477644delinsAATTT	GRCh37
NC_000012.10:g.87001771_87001775delinsAATTT	NCBI36
NG_008417.1:g.63350_63354delinsAAATT
NG_008417.2:g.63350_63354delinsAAATT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000309041.12:c.4792_4796delinsAAATT	ENSP00000308021.8:p.Lys1598=
ENST00000547691.8:c.2076_2080delinsAAATT
ENST00000552810.6:c.4792_4796delinsAAATT MANE Select	ENSP00000448012.1:p.Lys1598=
ENST00000672414.2:c.*2963_*2967delinsAAATT	ENSP00000500729.1:n.*2963_*2967delinsAAATT
ENST00000672647.1:n.3152_3156delinsAAATT
ENST00000673058.2:c.4792_4796delinsAAATT	ENSP00000500665.2:p.Lys1598=
ENST00000674971.1:c.4792_4796delinsAAATT	ENSP00000502194.1:p.Lys1598=
ENST00000675230.1:c.4771_4775delinsAAATT	ENSP00000502503.1:p.Lys1591=
ENST00000675408.1:c.4792_4796delinsAAATT	ENSP00000502298.1:p.Lys1598=
ENST00000675476.1:c.5653_5657delinsAAATT	ENSP00000502161.1:p.Lys1885=
ENST00000675628.1:n.5019_5023delinsAAATT
ENST00000675794.1:c.*2963_*2967delinsAAATT	ENSP00000502841.1:n.*2963_*2967delinsAAATT
ENST00000675833.1:c.5560_5564delinsAAATT	ENSP00000502559.1:p.Lys1854=
ENST00000675894.1:n.1097_1101delinsAAATT
ENST00000676074.1:c.4792_4796delinsAAATT	ENSP00000502079.1:p.Lys1598=
ENST00000676181.1:n.3720_3724delinsAAATT
ENST00000676363.1:n.10518_10522delinsAAATT
ENST00000676448.1:c.*2705_*2709delinsAAATT	ENSP00000501987.1:n.*2705_*2709delinsAAATT
ENST00000309041.11:c.4798_4802delinsAAATT	ENSP00000308021.7:p.Lys1600=
ENST00000547691.6:c.1972_1976delinsAAATT	ENSP00000446905.1:p.Lys658=
ENST00000552810.5:c.4792_4796delinsAAATT	ENSP00000448012.1:p.Lys1598=
NM_025114.3:c.4792_4796delinsAAATT	NP_079390.3:p.Lys1598=
XM_011538756.1:c.5653_5657delinsAAATT	XP_011537058.1:p.Lys1885=
XM_011538757.1:c.5653_5657delinsAAATT	XP_011537059.1:p.Lys1885=
XM_011538758.1:c.5653_5657delinsAAATT	XP_011537060.1:p.Lys1885=
XM_011538759.1:c.5653_5657delinsAAATT	XP_011537061.1:p.Lys1885=
XM_011538760.1:c.5653_5657delinsAAATT	XP_011537062.1:p.Lys1885=
XM_011538761.1:c.5653_5657delinsAAATT	XP_011537063.1:p.Lys1885=
XM_011538762.1:c.4885_4889delinsAAATT	XP_011537064.1:p.Lys1629=
XM_011538763.1:c.4792_4796delinsAAATT	XP_011537065.1:p.Lys1598=
XM_011538764.1:c.5653_5657delinsAAATT	XP_011537066.1:p.Lys1885=
XM_011538765.1:c.5653_5657delinsAAATT	XP_011537067.1:p.Lys1885=
XM_011538766.1:c.4114_4118delinsAAATT	XP_011537068.1:p.Lys1372=
XM_011538756.3:c.5653_5657delinsAAATT	XP_011537058.1:p.Lys1885=
XM_011538757.3:c.5653_5657delinsAAATT	XP_011537059.1:p.Lys1885=
XM_011538758.3:c.5653_5657delinsAAATT	XP_011537060.1:p.Lys1885=
XM_011538759.2:c.5653_5657delinsAAATT	XP_011537061.1:p.Lys1885=
XM_011538760.2:c.5653_5657delinsAAATT	XP_011537062.1:p.Lys1885=
XM_011538761.2:c.5653_5657delinsAAATT	XP_011537063.1:p.Lys1885=
XM_011538762.3:c.4885_4889delinsAAATT	XP_011537064.1:p.Lys1629=
XM_011538763.3:c.4792_4796delinsAAATT	XP_011537065.1:p.Lys1598=
XM_011538764.3:c.5653_5657delinsAAATT	XP_011537066.1:p.Lys1885=
XM_011538765.3:c.5653_5657delinsAAATT	XP_011537067.1:p.Lys1885=
XM_011538766.3:c.4114_4118delinsAAATT	XP_011537068.1:p.Lys1372=
XM_017019980.2:c.5653_5657delinsAAATT	XP_016875469.1:p.Lys1885=
XM_017019981.2:c.5653_5657delinsAAATT	XP_016875470.1:p.Lys1885=
XM_017019982.1:c.5653_5657delinsAAATT	XP_016875471.1:p.Lys1885=
XM_017019983.2:c.4771_4775delinsAAATT	XP_016875472.1:p.Lys1591=
XR_001748869.1:n.5997_6001delinsAAATT
XR_001748870.2:n.5997_6001delinsAAATT
NM_025114.4:c.4792_4796delinsAAATT MANE Select	NP_079390.3:p.Lys1598=