Canonical Allele Identifier: CA241153087
Gene: CEP290 HGNC NCBI

Linked Data

ClinVar Variation Id: 1078893
ClinVar RCV Id: RCV001393963
dbSNP Id: rs1019366465

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.88077212C>T , CM000674.2:g.88077212C>T GRCh38
NC_000012.11:g.88470989C>T , CM000674.1:g.88470989C>T GRCh37
NC_000012.10:g.86995120C>T NCBI36
NG_008417.1:g.70005G>A
NG_008417.2:g.70005G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000309041.12:c.5709+10G>A ENSP00000308021.8:n.5709+10G>A
ENST00000547691.8:c.2993+10G>A
ENST00000552810.6:c.5709+10G>A MANE Select ENSP00000448012.1:n.5709+10G>A
ENST00000672414.2:c.*3880+10G>A ENSP00000500729.1:n.*3880+10G>A
ENST00000672647.1:n.4069+10G>A
ENST00000673058.2:c.5709+10G>A ENSP00000500665.2:n.5709+10G>A
ENST00000674971.1:c.5709+10G>A ENSP00000502194.1:n.5709+10G>A
ENST00000675230.1:c.5688+10G>A ENSP00000502503.1:n.5688+10G>A
ENST00000675408.1:c.5709+10G>A ENSP00000502298.1:n.5709+10G>A
ENST00000675476.1:c.6570+10G>A ENSP00000502161.1:n.6570+10G>A
ENST00000675628.1:n.5936+10G>A
ENST00000675794.1:c.*3880+10G>A ENSP00000502841.1:n.*3880+10G>A
ENST00000675833.1:c.6477+10G>A ENSP00000502559.1:n.6477+10G>A
ENST00000675894.1:n.2014+10G>A
ENST00000676074.1:c.5709+10G>A ENSP00000502079.1:n.5709+10G>A
ENST00000676181.1:n.4637+10G>A
ENST00000676363.1:n.11435+10G>A
ENST00000676448.1:c.*3622+10G>A ENSP00000501987.1:n.*3622+10G>A
ENST00000309041.11:c.5715+10G>A ENSP00000308021.7:n.5715+10G>A
ENST00000547691.6:c.2889+10G>A ENSP00000446905.1:n.2889+10G>A
ENST00000552810.5:c.5709+10G>A ENSP00000448012.1:n.5709+10G>A
NM_025114.3:c.5709+10G>A NP_079390.3:n.5709+10G>A
XM_011538756.1:c.6570+10G>A XP_011537058.1:n.6570+10G>A
XM_011538757.1:c.6570+10G>A XP_011537059.1:n.6570+10G>A
XM_011538758.1:c.6570+10G>A XP_011537060.1:n.6570+10G>A
XM_011538759.1:c.6570+10G>A XP_011537061.1:n.6570+10G>A
XM_011538760.1:c.6570+10G>A XP_011537062.1:n.6570+10G>A
XM_011538761.1:c.6570+10G>A XP_011537063.1:n.6570+10G>A
XM_011538762.1:c.5802+10G>A XP_011537064.1:n.5802+10G>A
XM_011538763.1:c.5709+10G>A XP_011537065.1:n.5709+10G>A
XM_011538764.1:c.6570+10G>A XP_011537066.1:n.6570+10G>A
XM_011538765.1:c.6570+10G>A XP_011537067.1:n.6570+10G>A
XM_011538766.1:c.5031+10G>A XP_011537068.1:n.5031+10G>A
XR_945163.1:n.968-5101C>T
XM_011538756.3:c.6570+10G>A XP_011537058.1:n.6570+10G>A
XM_011538757.3:c.6570+10G>A XP_011537059.1:n.6570+10G>A
XM_011538758.3:c.6570+10G>A XP_011537060.1:n.6570+10G>A
XM_011538759.2:c.6570+10G>A XP_011537061.1:n.6570+10G>A
XM_011538760.2:c.6570+10G>A XP_011537062.1:n.6570+10G>A
XM_011538761.2:c.6570+10G>A XP_011537063.1:n.6570+10G>A
XM_011538762.3:c.5802+10G>A XP_011537064.1:n.5802+10G>A
XM_011538763.3:c.5709+10G>A XP_011537065.1:n.5709+10G>A
XM_011538764.3:c.6570+10G>A XP_011537066.1:n.6570+10G>A
XM_011538765.3:c.6570+10G>A XP_011537067.1:n.6570+10G>A
XM_011538766.3:c.5031+10G>A XP_011537068.1:n.5031+10G>A
XM_017019980.2:c.6570+10G>A XP_016875469.1:n.6570+10G>A
XM_017019981.2:c.6570+10G>A XP_016875470.1:n.6570+10G>A
XM_017019982.1:c.6570+10G>A XP_016875471.1:n.6570+10G>A
XM_017019983.2:c.5688+10G>A XP_016875472.1:n.5688+10G>A
XR_001748869.1:n.6914+10G>A
XR_001748870.2:n.6914+10G>A
NM_025114.4:c.5709+10G>A MANE Select NP_079390.3:n.5709+10G>A