Canonical Allele Identifier: CA277788

Gene: CEP290

Linked Data - Expert Curation

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.88118537dup , CM000674.2:g.88118537dup	GRCh38
NC_000012.11:g.88512314dup , CM000674.1:g.88512314dup	GRCh37
NC_000012.10:g.87036445dup	NCBI36
NG_008417.1:g.28689dup
NG_008417.2:g.28689dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000309041.12:c.1666dup	ENSP00000308021.8:p.Ile556AsnfsTer20
ENST00000397838.8:c.1612dup	ENSP00000380938.5:p.Ile538AsnfsTer20
ENST00000547926.7:c.1666dup	ENSP00000448573.3:p.Ile556AsnfsTer20
ENST00000552810.6:c.1666dup MANE Select	ENSP00000448012.1:p.Ile556AsnfsTer20
ENST00000671822.2:n.3335dup
ENST00000672414.2:c.1666dup	ENSP00000500729.1:p.Ile556AsnfsTer24
ENST00000673058.2:c.1666dup	ENSP00000500665.2:p.Ile556AsnfsTer20
ENST00000674971.1:c.1666dup	ENSP00000502194.1:p.Ile556AsnfsTer20
ENST00000675230.1:c.1645dup	ENSP00000502503.1:p.Ile549AsnfsTer20
ENST00000675408.1:c.1666dup	ENSP00000502298.1:p.Ile556AsnfsTer20
ENST00000675476.1:c.1666dup	ENSP00000502161.1:p.Ile556AsnfsTer20
ENST00000675559.1:c.*212dup	ENSP00000502163.1:n.*212dup
ENST00000675628.1:n.1893dup
ENST00000675794.1:c.1666dup	ENSP00000502841.1:p.Ile556AsnfsTer24
ENST00000675833.1:c.1666dup	ENSP00000502559.1:p.Ile556AsnfsTer20
ENST00000676074.1:c.1666dup	ENSP00000502079.1:p.Ile556AsnfsTer20
ENST00000676351.1:c.*2621dup	ENSP00000502046.1:n.*2621dup
ENST00000676363.1:n.3729dup
ENST00000676418.1:c.*123dup	ENSP00000502371.1:n.*123dup
ENST00000676448.1:c.1666dup	ENSP00000501987.1:p.Ile556AsnfsTer20
ENST00000309041.11:c.1672dup	ENSP00000308021.7:p.Ile558AsnfsTer20
ENST00000397838.7:c.1672dup	ENSP00000380938.4:p.Ile558AsnfsTer20
ENST00000547926.6:c.1564dup	ENSP00000448573.2:p.Ile522AsnfsTer20
ENST00000552810.5:c.1666dup	ENSP00000448012.1:p.Ile556AsnfsTer20
ENST00000604024.5:c.832dup	ENSP00000473863.1:p.Ile278AsnfsTer20
NM_025114.3:c.1666dup	NP_079390.3:p.Ile556AsnfsTer20
XM_011538756.1:c.1666dup	XP_011537058.1:p.Ile556AsnfsTer20
XM_011538757.1:c.1666dup	XP_011537059.1:p.Ile556AsnfsTer20
XM_011538758.1:c.1666dup	XP_011537060.1:p.Ile556AsnfsTer20
XM_011538759.1:c.1666dup	XP_011537061.1:p.Ile556AsnfsTer20
XM_011538760.1:c.1666dup	XP_011537062.1:p.Ile556AsnfsTer20
XM_011538761.1:c.1666dup	XP_011537063.1:p.Ile556AsnfsTer20
XM_011538762.1:c.1666dup	XP_011537064.1:p.Ile556AsnfsTer20
XM_011538763.1:c.1666dup	XP_011537065.1:p.Ile556AsnfsTer20
XM_011538764.1:c.1666dup	XP_011537066.1:p.Ile556AsnfsTer20
XM_011538765.1:c.1666dup	XP_011537067.1:p.Ile556AsnfsTer20
XM_011538766.1:c.127dup	XP_011537068.1:p.Ile43AsnfsTer20
XM_011538756.3:c.1666dup	XP_011537058.1:p.Ile556AsnfsTer20
XM_011538757.3:c.1666dup	XP_011537059.1:p.Ile556AsnfsTer20
XM_011538758.3:c.1666dup	XP_011537060.1:p.Ile556AsnfsTer20
XM_011538759.2:c.1666dup	XP_011537061.1:p.Ile556AsnfsTer20
XM_011538760.2:c.1666dup	XP_011537062.1:p.Ile556AsnfsTer20
XM_011538761.2:c.1666dup	XP_011537063.1:p.Ile556AsnfsTer20
XM_011538762.3:c.1666dup	XP_011537064.1:p.Ile556AsnfsTer20
XM_011538763.3:c.1666dup	XP_011537065.1:p.Ile556AsnfsTer20
XM_011538764.3:c.1666dup	XP_011537066.1:p.Ile556AsnfsTer20
XM_011538765.3:c.1666dup	XP_011537067.1:p.Ile556AsnfsTer20
XM_011538766.3:c.127dup	XP_011537068.1:p.Ile43AsnfsTer20
XM_017019980.2:c.1666dup	XP_016875469.1:p.Ile556AsnfsTer20
XM_017019981.2:c.1666dup	XP_016875470.1:p.Ile556AsnfsTer20
XM_017019982.1:c.1666dup	XP_016875471.1:p.Ile556AsnfsTer20
XM_017019983.2:c.1645dup	XP_016875472.1:p.Ile549AsnfsTer20
XR_001748869.1:n.2010dup
XR_001748870.2:n.2010dup
NM_025114.4:c.1666dup MANE Select	NP_079390.3:p.Ile556AsnfsTer20