Canonical Allele Identifier: CA386007180
Community Standard Title: NM_025114.4(CEP290):c.3013G>T (p.Glu1005Ter)
Gene: CEP290 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.88096978C>A , CM000674.2:g.88096978C>A GRCh38
NC_000012.11:g.88490755C>A , CM000674.1:g.88490755C>A GRCh37
NC_000012.10:g.87014886C>A NCBI36
NG_008417.1:g.50239G>T
NG_008417.2:g.50239G>T

Transcript Alleles

HGVS Amino-acid Change
NM_025114.4:c.3013G>T MANE Select NP_079390.3:p.Glu1005Ter
ENST00000552810.6:c.3013G>T MANE Select ENSP00000448012.1:p.Glu1005Ter
NM_025114.3:c.3013G>T NP_079390.3:p.Glu1005Ter
ENST00000309041.11:c.3019G>T ENSP00000308021.7:p.Glu1007Ter
ENST00000309041.12:c.3013G>T ENSP00000308021.8:p.Glu1005Ter
ENST00000547691.6:c.193G>T ENSP00000446905.1:p.Glu65Ter
ENST00000547691.8:c.297G>T
ENST00000552810.5:c.3013G>T ENSP00000448012.1:p.Glu1005Ter
ENST00000604024.5:c.2272G>T ENSP00000473863.1:p.Glu758Ter
ENST00000672414.2:c.*1184G>T ENSP00000500729.1:n.*1184G>T
ENST00000672647.1:n.1373G>T
ENST00000673058.2:c.3013G>T ENSP00000500665.2:p.Glu1005Ter
ENST00000674971.1:c.3013G>T ENSP00000502194.1:p.Glu1005Ter
ENST00000675089.1:c.196G>T ENSP00000501582.1:p.Glu66Ter
ENST00000675230.1:c.2992G>T ENSP00000502503.1:p.Glu998Ter
ENST00000675408.1:c.3013G>T ENSP00000502298.1:p.Glu1005Ter
ENST00000675476.1:c.3874G>T ENSP00000502161.1:p.Glu1292Ter
ENST00000675628.1:n.3240G>T
ENST00000675794.1:c.*1184G>T ENSP00000502841.1:n.*1184G>T
ENST00000675833.1:c.3781G>T ENSP00000502559.1:p.Glu1261Ter
ENST00000676074.1:c.3013G>T ENSP00000502079.1:p.Glu1005Ter
ENST00000676181.1:n.701G>T
ENST00000676363.1:n.8739G>T
ENST00000676448.1:c.*926G>T ENSP00000501987.1:n.*926G>T
XM_011538756.1:c.3874G>T XP_011537058.1:p.Glu1292Ter
XM_011538756.3:c.3874G>T XP_011537058.1:p.Glu1292Ter
XM_011538757.1:c.3874G>T XP_011537059.1:p.Glu1292Ter
XM_011538757.3:c.3874G>T XP_011537059.1:p.Glu1292Ter
XM_011538758.1:c.3874G>T XP_011537060.1:p.Glu1292Ter
XM_011538758.3:c.3874G>T XP_011537060.1:p.Glu1292Ter
XM_011538759.1:c.3874G>T XP_011537061.1:p.Glu1292Ter
XM_011538759.2:c.3874G>T XP_011537061.1:p.Glu1292Ter
XM_011538760.1:c.3874G>T XP_011537062.1:p.Glu1292Ter
XM_011538760.2:c.3874G>T XP_011537062.1:p.Glu1292Ter
XM_011538761.1:c.3874G>T XP_011537063.1:p.Glu1292Ter
XM_011538761.2:c.3874G>T XP_011537063.1:p.Glu1292Ter
XM_011538762.1:c.3106G>T XP_011537064.1:p.Glu1036Ter
XM_011538762.3:c.3106G>T XP_011537064.1:p.Glu1036Ter
XM_011538763.1:c.3013G>T XP_011537065.1:p.Glu1005Ter
XM_011538763.3:c.3013G>T XP_011537065.1:p.Glu1005Ter
XM_011538764.1:c.3874G>T XP_011537066.1:p.Glu1292Ter
XM_011538764.3:c.3874G>T XP_011537066.1:p.Glu1292Ter
XM_011538765.1:c.3874G>T XP_011537067.1:p.Glu1292Ter
XM_011538765.3:c.3874G>T XP_011537067.1:p.Glu1292Ter
XM_011538766.1:c.2335G>T XP_011537068.1:p.Glu779Ter
XM_011538766.3:c.2335G>T XP_011537068.1:p.Glu779Ter
XM_017019980.2:c.3874G>T XP_016875469.1:p.Glu1292Ter
XM_017019981.2:c.3874G>T XP_016875470.1:p.Glu1292Ter
XM_017019982.1:c.3874G>T XP_016875471.1:p.Glu1292Ter
XM_017019983.2:c.2992G>T XP_016875472.1:p.Glu998Ter
XR_001748869.1:n.4218G>T
XR_001748870.2:n.4218G>T