Canonical Allele Identifier: CA233679
Gene: CEP290 HGNC NCBI

Linked Data

ClinVar Variation Id: 166837
dbSNP Id: rs727503855

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.88118536_88118537del , CM000674.2:g.88118536_88118537del GRCh38
NC_000012.11:g.88512313_88512314del , CM000674.1:g.88512313_88512314del GRCh37
NC_000012.10:g.87036444_87036445del NCBI36
NG_008417.1:g.28688_28689del
NG_008417.2:g.28688_28689del

Transcript Alleles

HGVS Amino-acid Change
ENST00000309041.12:c.1665_1666del ENSP00000308021.8:p.Lys555AsnfsTer20
ENST00000397838.8:c.1611_1612del ENSP00000380938.5:p.Lys537AsnfsTer20
ENST00000547926.7:c.1665_1666del ENSP00000448573.3:p.Lys555AsnfsTer20
ENST00000552810.6:c.1665_1666del MANE Select ENSP00000448012.1:p.Lys555AsnfsTer20
ENST00000671822.2:n.3334_3335del
ENST00000672414.2:c.1665_1666del ENSP00000500729.1:p.Lys555AsnfsTer24
ENST00000673058.2:c.1665_1666del ENSP00000500665.2:p.Lys555AsnfsTer20
ENST00000674971.1:c.1665_1666del ENSP00000502194.1:p.Lys555AsnfsTer20
ENST00000675230.1:c.1644_1645del ENSP00000502503.1:p.Lys548AsnfsTer20
ENST00000675408.1:c.1665_1666del ENSP00000502298.1:p.Lys555AsnfsTer20
ENST00000675476.1:c.1665_1666del ENSP00000502161.1:p.Lys555AsnfsTer20
ENST00000675559.1:c.*211_*212del ENSP00000502163.1:n.*211_*212del
ENST00000675628.1:n.1892_1893del
ENST00000675794.1:c.1665_1666del ENSP00000502841.1:p.Lys555AsnfsTer24
ENST00000675833.1:c.1665_1666del ENSP00000502559.1:p.Lys555AsnfsTer20
ENST00000676074.1:c.1665_1666del ENSP00000502079.1:p.Lys555AsnfsTer20
ENST00000676351.1:c.*2620_*2621del ENSP00000502046.1:n.*2620_*2621del
ENST00000676363.1:n.3728_3729del
ENST00000676418.1:c.*122_*123del ENSP00000502371.1:n.*122_*123del
ENST00000676448.1:c.1665_1666del ENSP00000501987.1:p.Lys555AsnfsTer20
ENST00000309041.11:c.1671_1672del ENSP00000308021.7:p.Lys557AsnfsTer20
ENST00000397838.7:c.1671_1672del ENSP00000380938.4:p.Lys557AsnfsTer20
ENST00000547926.6:c.1563_1564del ENSP00000448573.2:p.Lys521AsnfsTer20
ENST00000552810.5:c.1665_1666del ENSP00000448012.1:p.Lys555AsnfsTer20
ENST00000604024.5:c.831_832del ENSP00000473863.1:p.Lys277AsnfsTer20
NM_025114.3:c.1665_1666del NP_079390.3:p.Lys555AsnfsTer20
XM_011538756.1:c.1665_1666del XP_011537058.1:p.Lys555AsnfsTer20
XM_011538757.1:c.1665_1666del XP_011537059.1:p.Lys555AsnfsTer20
XM_011538758.1:c.1665_1666del XP_011537060.1:p.Lys555AsnfsTer20
XM_011538759.1:c.1665_1666del XP_011537061.1:p.Lys555AsnfsTer20
XM_011538760.1:c.1665_1666del XP_011537062.1:p.Lys555AsnfsTer20
XM_011538761.1:c.1665_1666del XP_011537063.1:p.Lys555AsnfsTer20
XM_011538762.1:c.1665_1666del XP_011537064.1:p.Lys555AsnfsTer20
XM_011538763.1:c.1665_1666del XP_011537065.1:p.Lys555AsnfsTer20
XM_011538764.1:c.1665_1666del XP_011537066.1:p.Lys555AsnfsTer20
XM_011538765.1:c.1665_1666del XP_011537067.1:p.Lys555AsnfsTer20
XM_011538766.1:c.126_127del XP_011537068.1:p.Lys42AsnfsTer20
XM_011538756.3:c.1665_1666del XP_011537058.1:p.Lys555AsnfsTer20
XM_011538757.3:c.1665_1666del XP_011537059.1:p.Lys555AsnfsTer20
XM_011538758.3:c.1665_1666del XP_011537060.1:p.Lys555AsnfsTer20
XM_011538759.2:c.1665_1666del XP_011537061.1:p.Lys555AsnfsTer20
XM_011538760.2:c.1665_1666del XP_011537062.1:p.Lys555AsnfsTer20
XM_011538761.2:c.1665_1666del XP_011537063.1:p.Lys555AsnfsTer20
XM_011538762.3:c.1665_1666del XP_011537064.1:p.Lys555AsnfsTer20
XM_011538763.3:c.1665_1666del XP_011537065.1:p.Lys555AsnfsTer20
XM_011538764.3:c.1665_1666del XP_011537066.1:p.Lys555AsnfsTer20
XM_011538765.3:c.1665_1666del XP_011537067.1:p.Lys555AsnfsTer20
XM_011538766.3:c.126_127del XP_011537068.1:p.Lys42AsnfsTer20
XM_017019980.2:c.1665_1666del XP_016875469.1:p.Lys555AsnfsTer20
XM_017019981.2:c.1665_1666del XP_016875470.1:p.Lys555AsnfsTer20
XM_017019982.1:c.1665_1666del XP_016875471.1:p.Lys555AsnfsTer20
XM_017019983.2:c.1644_1645del XP_016875472.1:p.Lys548AsnfsTer20
XR_001748869.1:n.2009_2010del
XR_001748870.2:n.2009_2010del
NM_025114.4:c.1665_1666del MANE Select NP_079390.3:p.Lys555AsnfsTer20