Canonical Allele Identifier: CA2052913820
Gene: CEP290 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.88077338G= , CM000674.2:g.88077338G= GRCh38
NC_000012.11:g.88471115G= , CM000674.1:g.88471115G= GRCh37
NC_000012.10:g.86995246G= NCBI36
NG_008417.1:g.69879C=
NG_008417.2:g.69879C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000309041.12:c.5593C= ENSP00000308021.8:p.Pro1865=
ENST00000547691.8:c.2877C=
ENST00000552810.6:c.5593C= MANE Select ENSP00000448012.1:p.Pro1865=
ENST00000672414.2:c.*3764C= ENSP00000500729.1:n.*3764C=
ENST00000672647.1:n.3953C=
ENST00000673058.2:c.5593C= ENSP00000500665.2:p.Pro1865=
ENST00000674971.1:c.5593C= ENSP00000502194.1:p.Pro1865=
ENST00000675230.1:c.5572C= ENSP00000502503.1:p.Pro1858=
ENST00000675408.1:c.5593C= ENSP00000502298.1:p.Pro1865=
ENST00000675476.1:c.6454C= ENSP00000502161.1:p.Pro2152=
ENST00000675628.1:n.5820C=
ENST00000675794.1:c.*3764C= ENSP00000502841.1:n.*3764C=
ENST00000675833.1:c.6361C= ENSP00000502559.1:p.Pro2121=
ENST00000675894.1:n.1898C=
ENST00000676074.1:c.5593C= ENSP00000502079.1:p.Pro1865=
ENST00000676181.1:n.4521C=
ENST00000676363.1:n.11319C=
ENST00000676448.1:c.*3506C= ENSP00000501987.1:n.*3506C=
ENST00000309041.11:c.5599C= ENSP00000308021.7:p.Pro1867=
ENST00000547691.6:c.2773C= ENSP00000446905.1:p.Pro925=
ENST00000552810.5:c.5593C= ENSP00000448012.1:p.Pro1865=
NM_025114.3:c.5593C= NP_079390.3:p.Pro1865=
XM_011538756.1:c.6454C= XP_011537058.1:p.Pro2152=
XM_011538757.1:c.6454C= XP_011537059.1:p.Pro2152=
XM_011538758.1:c.6454C= XP_011537060.1:p.Pro2152=
XM_011538759.1:c.6454C= XP_011537061.1:p.Pro2152=
XM_011538760.1:c.6454C= XP_011537062.1:p.Pro2152=
XM_011538761.1:c.6454C= XP_011537063.1:p.Pro2152=
XM_011538762.1:c.5686C= XP_011537064.1:p.Pro1896=
XM_011538763.1:c.5593C= XP_011537065.1:p.Pro1865=
XM_011538764.1:c.6454C= XP_011537066.1:p.Pro2152=
XM_011538765.1:c.6454C= XP_011537067.1:p.Pro2152=
XM_011538766.1:c.4915C= XP_011537068.1:p.Pro1639=
XR_945163.1:n.968-4975G=
XM_011538756.3:c.6454C= XP_011537058.1:p.Pro2152=
XM_011538757.3:c.6454C= XP_011537059.1:p.Pro2152=
XM_011538758.3:c.6454C= XP_011537060.1:p.Pro2152=
XM_011538759.2:c.6454C= XP_011537061.1:p.Pro2152=
XM_011538760.2:c.6454C= XP_011537062.1:p.Pro2152=
XM_011538761.2:c.6454C= XP_011537063.1:p.Pro2152=
XM_011538762.3:c.5686C= XP_011537064.1:p.Pro1896=
XM_011538763.3:c.5593C= XP_011537065.1:p.Pro1865=
XM_011538764.3:c.6454C= XP_011537066.1:p.Pro2152=
XM_011538765.3:c.6454C= XP_011537067.1:p.Pro2152=
XM_011538766.3:c.4915C= XP_011537068.1:p.Pro1639=
XM_017019980.2:c.6454C= XP_016875469.1:p.Pro2152=
XM_017019981.2:c.6454C= XP_016875470.1:p.Pro2152=
XM_017019982.1:c.6454C= XP_016875471.1:p.Pro2152=
XM_017019983.2:c.5572C= XP_016875472.1:p.Pro1858=
XR_001748869.1:n.6798C=
XR_001748870.2:n.6798C=
NM_025114.4:c.5593C= MANE Select NP_079390.3:p.Pro1865=