Canonical Allele Identifier: CA277810
Gene: CEP290 HGNC NCBI

Linked Data

ClinVar Variation Id: 217636
dbSNP Id: rs575767207

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.88079112G>A , CM000674.2:g.88079112G>A GRCh38
NC_000012.11:g.88472889G>A , CM000674.1:g.88472889G>A GRCh37
NC_000012.10:g.86997020G>A NCBI36
NG_008417.1:g.68105C>T
NG_008417.2:g.68105C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000309041.12:c.5344C>T ENSP00000308021.8:p.Arg1782Ter
ENST00000547691.8:c.2628C>T
ENST00000552810.6:c.5344C>T MANE Select ENSP00000448012.1:p.Arg1782Ter
ENST00000672414.2:c.*3515C>T ENSP00000500729.1:n.*3515C>T
ENST00000672647.1:n.3704C>T
ENST00000673058.2:c.5344C>T ENSP00000500665.2:p.Arg1782Ter
ENST00000674971.1:c.5344C>T ENSP00000502194.1:p.Arg1782Ter
ENST00000675230.1:c.5323C>T ENSP00000502503.1:p.Arg1775Ter
ENST00000675408.1:c.5344C>T ENSP00000502298.1:p.Arg1782Ter
ENST00000675476.1:c.6205C>T ENSP00000502161.1:p.Arg2069Ter
ENST00000675628.1:n.5571C>T
ENST00000675794.1:c.*3515C>T ENSP00000502841.1:n.*3515C>T
ENST00000675833.1:c.6112C>T ENSP00000502559.1:p.Arg2038Ter
ENST00000675894.1:n.1649C>T
ENST00000676074.1:c.5344C>T ENSP00000502079.1:p.Arg1782Ter
ENST00000676181.1:n.4272C>T
ENST00000676363.1:n.11070C>T
ENST00000676448.1:c.*3257C>T ENSP00000501987.1:n.*3257C>T
ENST00000309041.11:c.5350C>T ENSP00000308021.7:p.Arg1784Ter
ENST00000547691.6:c.2524C>T ENSP00000446905.1:p.Arg842Ter
ENST00000552810.5:c.5344C>T ENSP00000448012.1:p.Arg1782Ter
NM_025114.3:c.5344C>T NP_079390.3:p.Arg1782Ter
XM_011538756.1:c.6205C>T XP_011537058.1:p.Arg2069Ter
XM_011538757.1:c.6205C>T XP_011537059.1:p.Arg2069Ter
XM_011538758.1:c.6205C>T XP_011537060.1:p.Arg2069Ter
XM_011538759.1:c.6205C>T XP_011537061.1:p.Arg2069Ter
XM_011538760.1:c.6205C>T XP_011537062.1:p.Arg2069Ter
XM_011538761.1:c.6205C>T XP_011537063.1:p.Arg2069Ter
XM_011538762.1:c.5437C>T XP_011537064.1:p.Arg1813Ter
XM_011538763.1:c.5344C>T XP_011537065.1:p.Arg1782Ter
XM_011538764.1:c.6205C>T XP_011537066.1:p.Arg2069Ter
XM_011538765.1:c.6205C>T XP_011537067.1:p.Arg2069Ter
XM_011538766.1:c.4666C>T XP_011537068.1:p.Arg1556Ter
XR_945163.1:n.968-3201G>A
XM_011538756.3:c.6205C>T XP_011537058.1:p.Arg2069Ter
XM_011538757.3:c.6205C>T XP_011537059.1:p.Arg2069Ter
XM_011538758.3:c.6205C>T XP_011537060.1:p.Arg2069Ter
XM_011538759.2:c.6205C>T XP_011537061.1:p.Arg2069Ter
XM_011538760.2:c.6205C>T XP_011537062.1:p.Arg2069Ter
XM_011538761.2:c.6205C>T XP_011537063.1:p.Arg2069Ter
XM_011538762.3:c.5437C>T XP_011537064.1:p.Arg1813Ter
XM_011538763.3:c.5344C>T XP_011537065.1:p.Arg1782Ter
XM_011538764.3:c.6205C>T XP_011537066.1:p.Arg2069Ter
XM_011538765.3:c.6205C>T XP_011537067.1:p.Arg2069Ter
XM_011538766.3:c.4666C>T XP_011537068.1:p.Arg1556Ter
XM_017019980.2:c.6205C>T XP_016875469.1:p.Arg2069Ter
XM_017019981.2:c.6205C>T XP_016875470.1:p.Arg2069Ter
XM_017019982.1:c.6205C>T XP_016875471.1:p.Arg2069Ter
XM_017019983.2:c.5323C>T XP_016875472.1:p.Arg1775Ter
XR_001748869.1:n.6549C>T
XR_001748870.2:n.6549C>T
NM_025114.4:c.5344C>T MANE Select NP_079390.3:p.Arg1782Ter