Canonical Allele Identifier: CA2052913809
Gene: CEP290 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.88077310A= , CM000674.2:g.88077310A= GRCh38
NC_000012.11:g.88471087A= , CM000674.1:g.88471087A= GRCh37
NC_000012.10:g.86995218A= NCBI36
NG_008417.1:g.69907T=
NG_008417.2:g.69907T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000309041.12:c.5621T= ENSP00000308021.8:p.Ile1874=
ENST00000547691.8:c.2905T=
ENST00000552810.6:c.5621T= MANE Select ENSP00000448012.1:p.Ile1874=
ENST00000672414.2:c.*3792T= ENSP00000500729.1:n.*3792T=
ENST00000672647.1:n.3981T=
ENST00000673058.2:c.5621T= ENSP00000500665.2:p.Ile1874=
ENST00000674971.1:c.5621T= ENSP00000502194.1:p.Ile1874=
ENST00000675230.1:c.5600T= ENSP00000502503.1:p.Ile1867=
ENST00000675408.1:c.5621T= ENSP00000502298.1:p.Ile1874=
ENST00000675476.1:c.6482T= ENSP00000502161.1:p.Ile2161=
ENST00000675628.1:n.5848T=
ENST00000675794.1:c.*3792T= ENSP00000502841.1:n.*3792T=
ENST00000675833.1:c.6389T= ENSP00000502559.1:p.Ile2130=
ENST00000675894.1:n.1926T=
ENST00000676074.1:c.5621T= ENSP00000502079.1:p.Ile1874=
ENST00000676181.1:n.4549T=
ENST00000676363.1:n.11347T=
ENST00000676448.1:c.*3534T= ENSP00000501987.1:n.*3534T=
ENST00000309041.11:c.5627T= ENSP00000308021.7:p.Ile1876=
ENST00000547691.6:c.2801T= ENSP00000446905.1:p.Ile934=
ENST00000552810.5:c.5621T= ENSP00000448012.1:p.Ile1874=
NM_025114.3:c.5621T= NP_079390.3:p.Ile1874=
XM_011538756.1:c.6482T= XP_011537058.1:p.Ile2161=
XM_011538757.1:c.6482T= XP_011537059.1:p.Ile2161=
XM_011538758.1:c.6482T= XP_011537060.1:p.Ile2161=
XM_011538759.1:c.6482T= XP_011537061.1:p.Ile2161=
XM_011538760.1:c.6482T= XP_011537062.1:p.Ile2161=
XM_011538761.1:c.6482T= XP_011537063.1:p.Ile2161=
XM_011538762.1:c.5714T= XP_011537064.1:p.Ile1905=
XM_011538763.1:c.5621T= XP_011537065.1:p.Ile1874=
XM_011538764.1:c.6482T= XP_011537066.1:p.Ile2161=
XM_011538765.1:c.6482T= XP_011537067.1:p.Ile2161=
XM_011538766.1:c.4943T= XP_011537068.1:p.Ile1648=
XR_945163.1:n.968-5003A=
XM_011538756.3:c.6482T= XP_011537058.1:p.Ile2161=
XM_011538757.3:c.6482T= XP_011537059.1:p.Ile2161=
XM_011538758.3:c.6482T= XP_011537060.1:p.Ile2161=
XM_011538759.2:c.6482T= XP_011537061.1:p.Ile2161=
XM_011538760.2:c.6482T= XP_011537062.1:p.Ile2161=
XM_011538761.2:c.6482T= XP_011537063.1:p.Ile2161=
XM_011538762.3:c.5714T= XP_011537064.1:p.Ile1905=
XM_011538763.3:c.5621T= XP_011537065.1:p.Ile1874=
XM_011538764.3:c.6482T= XP_011537066.1:p.Ile2161=
XM_011538765.3:c.6482T= XP_011537067.1:p.Ile2161=
XM_011538766.3:c.4943T= XP_011537068.1:p.Ile1648=
XM_017019980.2:c.6482T= XP_016875469.1:p.Ile2161=
XM_017019981.2:c.6482T= XP_016875470.1:p.Ile2161=
XM_017019982.1:c.6482T= XP_016875471.1:p.Ile2161=
XM_017019983.2:c.5600T= XP_016875472.1:p.Ile1867=
XR_001748869.1:n.6826T=
XR_001748870.2:n.6826T=
NM_025114.4:c.5621T= MANE Select NP_079390.3:p.Ile1874=