Canonical Allele Identifier: CA6711788
Community Standard Title: NM_025114.4(CEP290):c.5129C>T (p.Ala1710Val)
Gene: CEP290 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.88080279G>A , CM000674.2:g.88080279G>A GRCh38
NC_000012.11:g.88474056G>A , CM000674.1:g.88474056G>A GRCh37
NC_000012.10:g.86998187G>A NCBI36
NG_008417.1:g.66938C>T
NG_008417.2:g.66938C>T

Transcript Alleles

HGVS Amino-acid Change
NM_025114.4:c.5129C>T MANE Select NP_079390.3:p.Ala1710Val
ENST00000552810.6:c.5129C>T MANE Select ENSP00000448012.1:p.Ala1710Val
NM_025114.3:c.5129C>T NP_079390.3:p.Ala1710Val
ENST00000309041.11:c.5135C>T ENSP00000308021.7:p.Ala1712Val
ENST00000309041.12:c.5129C>T ENSP00000308021.8:p.Ala1710Val
ENST00000547691.6:c.2309C>T ENSP00000446905.1:p.Ala770Val
ENST00000547691.8:c.2413C>T
ENST00000552810.5:c.5129C>T ENSP00000448012.1:p.Ala1710Val
ENST00000672414.2:c.*3300C>T ENSP00000500729.1:n.*3300C>T
ENST00000672647.1:n.3489C>T
ENST00000673058.2:c.5129C>T ENSP00000500665.2:p.Ala1710Val
ENST00000674971.1:c.5129C>T ENSP00000502194.1:p.Ala1710Val
ENST00000675230.1:c.5108C>T ENSP00000502503.1:p.Ala1703Val
ENST00000675408.1:c.5129C>T ENSP00000502298.1:p.Ala1710Val
ENST00000675476.1:c.5990C>T ENSP00000502161.1:p.Ala1997Val
ENST00000675628.1:n.5356C>T
ENST00000675794.1:c.*3300C>T ENSP00000502841.1:n.*3300C>T
ENST00000675833.1:c.5897C>T ENSP00000502559.1:p.Ala1966Val
ENST00000675894.1:n.1434C>T
ENST00000676074.1:c.5129C>T ENSP00000502079.1:p.Ala1710Val
ENST00000676181.1:n.4057C>T
ENST00000676363.1:n.10855C>T
ENST00000676448.1:c.*3042C>T ENSP00000501987.1:n.*3042C>T
XM_011538756.1:c.5990C>T XP_011537058.1:p.Ala1997Val
XM_011538756.3:c.5990C>T XP_011537058.1:p.Ala1997Val
XM_011538757.1:c.5990C>T XP_011537059.1:p.Ala1997Val
XM_011538757.3:c.5990C>T XP_011537059.1:p.Ala1997Val
XM_011538758.1:c.5990C>T XP_011537060.1:p.Ala1997Val
XM_011538758.3:c.5990C>T XP_011537060.1:p.Ala1997Val
XM_011538759.1:c.5990C>T XP_011537061.1:p.Ala1997Val
XM_011538759.2:c.5990C>T XP_011537061.1:p.Ala1997Val
XM_011538760.1:c.5990C>T XP_011537062.1:p.Ala1997Val
XM_011538760.2:c.5990C>T XP_011537062.1:p.Ala1997Val
XM_011538761.1:c.5990C>T XP_011537063.1:p.Ala1997Val
XM_011538761.2:c.5990C>T XP_011537063.1:p.Ala1997Val
XM_011538762.1:c.5222C>T XP_011537064.1:p.Ala1741Val
XM_011538762.3:c.5222C>T XP_011537064.1:p.Ala1741Val
XM_011538763.1:c.5129C>T XP_011537065.1:p.Ala1710Val
XM_011538763.3:c.5129C>T XP_011537065.1:p.Ala1710Val
XM_011538764.1:c.5990C>T XP_011537066.1:p.Ala1997Val
XM_011538764.3:c.5990C>T XP_011537066.1:p.Ala1997Val
XM_011538765.1:c.5990C>T XP_011537067.1:p.Ala1997Val
XM_011538765.3:c.5990C>T XP_011537067.1:p.Ala1997Val
XM_011538766.1:c.4451C>T XP_011537068.1:p.Ala1484Val
XM_011538766.3:c.4451C>T XP_011537068.1:p.Ala1484Val
XM_017019980.2:c.5990C>T XP_016875469.1:p.Ala1997Val
XM_017019981.2:c.5990C>T XP_016875470.1:p.Ala1997Val
XM_017019982.1:c.5990C>T XP_016875471.1:p.Ala1997Val
XM_017019983.2:c.5108C>T XP_016875472.1:p.Ala1703Val
XR_001748869.1:n.6334C>T
XR_001748870.2:n.6334C>T
XR_945163.1:n.968-2034G>A