Canonical Allele Identifier: CA2052907547

Gene: CEP290

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.88062771_88062772delinsAC , CM000674.2:g.88062771_88062772delinsAC	GRCh38
NC_000012.11:g.88456548_88456549delinsAC , CM000674.1:g.88456548_88456549delinsAC	GRCh37
NC_000012.10:g.86980679_86980680delinsAC	NCBI36
NG_008417.1:g.84445_84446delinsGT
NG_008417.2:g.84445_84446delinsGT

Transcript Alleles

HGVS	Amino-acid change
ENST00000309041.12:c.6286_6287delinsGT	ENSP00000308021.8:p.Val2096=
ENST00000547691.8:c.3561_3562delinsGT
ENST00000552810.6:c.6277_6278delinsGT MANE Select	ENSP00000448012.1:p.Val2093=
ENST00000672414.2:c.*4448_*4449delinsGT	ENSP00000500729.1:n.*4448_*4449delinsGT
ENST00000672647.1:n.4637_4638delinsGT
ENST00000673058.2:c.6277_6278delinsGT	ENSP00000500665.2:p.Val2093=
ENST00000674889.1:n.3230_3231delinsGT
ENST00000674971.1:c.6277_6278delinsGT	ENSP00000502194.1:p.Val2093=
ENST00000675230.1:c.6256_6257delinsGT	ENSP00000502503.1:p.Val2086=
ENST00000675408.1:c.6277_6278delinsGT	ENSP00000502298.1:p.Val2093=
ENST00000675476.1:c.7138_7139delinsGT	ENSP00000502161.1:p.Val2380=
ENST00000675628.1:n.6504_6505delinsGT
ENST00000675794.1:c.*4448_*4449delinsGT	ENSP00000502841.1:n.*4448_*4449delinsGT
ENST00000675833.1:c.7045_7046delinsGT	ENSP00000502559.1:p.Val2349=
ENST00000675894.1:n.2582_2583delinsGT
ENST00000676074.1:c.6277_6278delinsGT	ENSP00000502079.1:p.Val2093=
ENST00000676181.1:n.5205_5206delinsGT
ENST00000676190.1:n.716_717delinsGT
ENST00000676363.1:n.12003_12004delinsGT
ENST00000309041.11:c.6283_6284delinsGT	ENSP00000308021.7:p.Val2095=
ENST00000547691.6:c.3457_3458delinsGT	ENSP00000446905.1:p.Val1153=
ENST00000552810.5:c.6277_6278delinsGT	ENSP00000448012.1:p.Val2093=
NM_025114.3:c.6277_6278delinsGT	NP_079390.3:p.Val2093=
XM_011538756.1:c.7147_7148delinsGT	XP_011537058.1:p.Val2383=
XM_011538757.1:c.7147_7148delinsGT	XP_011537059.1:p.Val2383=
XM_011538758.1:c.7144_7145delinsGT	XP_011537060.1:p.Val2382=
XM_011538759.1:c.7138_7139delinsGT	XP_011537061.1:p.Val2380=
XM_011538760.1:c.7147_7148delinsGT	XP_011537062.1:p.Val2383=
XM_011538761.1:c.7147_7148delinsGT	XP_011537063.1:p.Val2383=
XM_011538762.1:c.6379_6380delinsGT	XP_011537064.1:p.Val2127=
XM_011538763.1:c.6286_6287delinsGT	XP_011537065.1:p.Val2096=
XM_011538766.1:c.5608_5609delinsGT	XP_011537068.1:p.Val1870=
XR_945163.1:n.967+5751_967+5752delinsAC
XM_011538756.3:c.7147_7148delinsGT	XP_011537058.1:p.Val2383=
XM_011538757.3:c.7147_7148delinsGT	XP_011537059.1:p.Val2383=
XM_011538758.3:c.7144_7145delinsGT	XP_011537060.1:p.Val2382=
XM_011538759.2:c.7138_7139delinsGT	XP_011537061.1:p.Val2380=
XM_011538760.2:c.7147_7148delinsGT	XP_011537062.1:p.Val2383=
XM_011538761.2:c.7147_7148delinsGT	XP_011537063.1:p.Val2383=
XM_011538762.3:c.6379_6380delinsGT	XP_011537064.1:p.Val2127=
XM_011538763.3:c.6286_6287delinsGT	XP_011537065.1:p.Val2096=
XM_011538766.3:c.5608_5609delinsGT	XP_011537068.1:p.Val1870=
XM_017019980.2:c.7138_7139delinsGT	XP_016875469.1:p.Val2380=
XM_017019981.2:c.7138_7139delinsGT	XP_016875470.1:p.Val2380=
XM_017019982.1:c.7147_7148delinsGT	XP_016875471.1:p.Val2383=
XM_017019983.2:c.6265_6266delinsGT	XP_016875472.1:p.Val2089=
XR_001748869.1:n.7482_7483delinsGT
XR_001748870.2:n.7482_7483delinsGT
NM_025114.4:c.6277_6278delinsGT MANE Select	NP_079390.3:p.Val2093=