Canonical Allele Identifier: CA2052914296

Gene: CEP290

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.88102768_88102769delinsTC , CM000674.2:g.88102768_88102769delinsTC	GRCh38
NC_000012.11:g.88496545_88496546delinsTC , CM000674.1:g.88496545_88496546delinsTC	GRCh37
NC_000012.10:g.87020676_87020677delinsTC	NCBI36
NG_008417.1:g.44448_44449delinsGA
NG_008417.2:g.44448_44449delinsGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000309041.12:c.2991+69_2991+70delinsGA	ENSP00000308021.8:n.2991+69_2991+70delinsGA
ENST00000547691.8:c.275+69_275+70delinsGA
ENST00000552810.6:c.2991+69_2991+70delinsGA MANE Select	ENSP00000448012.1:n.2991+69_2991+70delinsGA
ENST00000672414.2:c.*1162+69_*1162+70delinsGA	ENSP00000500729.1:n.*1162+69_*1162+70delinsGA
ENST00000672647.1:n.1351+69_1351+70delinsGA
ENST00000673058.2:c.2991+69_2991+70delinsGA	ENSP00000500665.2:n.2991+69_2991+70delinsGA
ENST00000674971.1:c.2991+69_2991+70delinsGA	ENSP00000502194.1:n.2991+69_2991+70delinsGA
ENST00000675089.1:c.174+69_174+70delinsGA	ENSP00000501582.1:n.174+69_174+70delinsGA
ENST00000675230.1:c.2970+69_2970+70delinsGA	ENSP00000502503.1:n.2970+69_2970+70delinsGA
ENST00000675408.1:c.2991+69_2991+70delinsGA	ENSP00000502298.1:n.2991+69_2991+70delinsGA
ENST00000675476.1:c.3852+69_3852+70delinsGA	ENSP00000502161.1:n.3852+69_3852+70delinsGA
ENST00000675628.1:n.3218+69_3218+70delinsGA
ENST00000675794.1:c.*1162+69_*1162+70delinsGA	ENSP00000502841.1:n.*1162+69_*1162+70delinsGA
ENST00000675833.1:c.3759+69_3759+70delinsGA	ENSP00000502559.1:n.3759+69_3759+70delinsGA
ENST00000676074.1:c.2991+69_2991+70delinsGA	ENSP00000502079.1:n.2991+69_2991+70delinsGA
ENST00000676181.1:n.679+69_679+70delinsGA
ENST00000676363.1:n.8717+69_8717+70delinsGA
ENST00000676448.1:c.*904+69_*904+70delinsGA	ENSP00000501987.1:n.*904+69_*904+70delinsGA
ENST00000309041.11:c.2997+69_2997+70delinsGA	ENSP00000308021.7:n.2997+69_2997+70delinsGA
ENST00000547691.6:c.171+69_171+70delinsGA	ENSP00000446905.1:n.171+69_171+70delinsGA
ENST00000552810.5:c.2991+69_2991+70delinsGA	ENSP00000448012.1:n.2991+69_2991+70delinsGA
ENST00000604024.5:c.2250+69_2250+70delinsGA	ENSP00000473863.1:n.2250+69_2250+70delinsGA
NM_025114.3:c.2991+69_2991+70delinsGA	NP_079390.3:n.2991+69_2991+70delinsGA
XM_011538756.1:c.3852+69_3852+70delinsGA	XP_011537058.1:n.3852+69_3852+70delinsGA
XM_011538757.1:c.3852+69_3852+70delinsGA	XP_011537059.1:n.3852+69_3852+70delinsGA
XM_011538758.1:c.3852+69_3852+70delinsGA	XP_011537060.1:n.3852+69_3852+70delinsGA
XM_011538759.1:c.3852+69_3852+70delinsGA	XP_011537061.1:n.3852+69_3852+70delinsGA
XM_011538760.1:c.3852+69_3852+70delinsGA	XP_011537062.1:n.3852+69_3852+70delinsGA
XM_011538761.1:c.3852+69_3852+70delinsGA	XP_011537063.1:n.3852+69_3852+70delinsGA
XM_011538762.1:c.3084+69_3084+70delinsGA	XP_011537064.1:n.3084+69_3084+70delinsGA
XM_011538763.1:c.2991+69_2991+70delinsGA	XP_011537065.1:n.2991+69_2991+70delinsGA
XM_011538764.1:c.3852+69_3852+70delinsGA	XP_011537066.1:n.3852+69_3852+70delinsGA
XM_011538765.1:c.3852+69_3852+70delinsGA	XP_011537067.1:n.3852+69_3852+70delinsGA
XM_011538766.1:c.2313+69_2313+70delinsGA	XP_011537068.1:n.2313+69_2313+70delinsGA
XM_011538756.3:c.3852+69_3852+70delinsGA	XP_011537058.1:n.3852+69_3852+70delinsGA
XM_011538757.3:c.3852+69_3852+70delinsGA	XP_011537059.1:n.3852+69_3852+70delinsGA
XM_011538758.3:c.3852+69_3852+70delinsGA	XP_011537060.1:n.3852+69_3852+70delinsGA
XM_011538759.2:c.3852+69_3852+70delinsGA	XP_011537061.1:n.3852+69_3852+70delinsGA
XM_011538760.2:c.3852+69_3852+70delinsGA	XP_011537062.1:n.3852+69_3852+70delinsGA
XM_011538761.2:c.3852+69_3852+70delinsGA	XP_011537063.1:n.3852+69_3852+70delinsGA
XM_011538762.3:c.3084+69_3084+70delinsGA	XP_011537064.1:n.3084+69_3084+70delinsGA
XM_011538763.3:c.2991+69_2991+70delinsGA	XP_011537065.1:n.2991+69_2991+70delinsGA
XM_011538764.3:c.3852+69_3852+70delinsGA	XP_011537066.1:n.3852+69_3852+70delinsGA
XM_011538765.3:c.3852+69_3852+70delinsGA	XP_011537067.1:n.3852+69_3852+70delinsGA
XM_011538766.3:c.2313+69_2313+70delinsGA	XP_011537068.1:n.2313+69_2313+70delinsGA
XM_017019980.2:c.3852+69_3852+70delinsGA	XP_016875469.1:n.3852+69_3852+70delinsGA
XM_017019981.2:c.3852+69_3852+70delinsGA	XP_016875470.1:n.3852+69_3852+70delinsGA
XM_017019982.1:c.3852+69_3852+70delinsGA	XP_016875471.1:n.3852+69_3852+70delinsGA
XM_017019983.2:c.2970+69_2970+70delinsGA	XP_016875472.1:n.2970+69_2970+70delinsGA
XR_001748869.1:n.4196+69_4196+70delinsGA
XR_001748870.2:n.4196+69_4196+70delinsGA
NM_025114.4:c.2991+69_2991+70delinsGA MANE Select	NP_079390.3:n.2991+69_2991+70delinsGA