Canonical Allele Identifier: CA2620108518

Gene: CEP290

Linked Data

• gnomAD v4: 12-88083897-ATC-A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.88083899_88083900del , CM000674.2:g.88083899_88083900del	GRCh38
NC_000012.11:g.88477676_88477677del , CM000674.1:g.88477676_88477677del	GRCh37
NC_000012.10:g.87001807_87001808del	NCBI36
NG_008417.1:g.63318_63319del
NG_008417.2:g.63318_63319del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000309041.12:c.4760_4761del	ENSP00000308021.8:p.Arg1587IlefsTer6
ENST00000547691.8:c.2044_2045del
ENST00000552810.6:c.4760_4761del MANE Select	ENSP00000448012.1:p.Arg1587IlefsTer6
ENST00000672414.2:c.*2931_*2932del	ENSP00000500729.1:n.*2931_*2932del
ENST00000672647.1:n.3120_3121del
ENST00000673058.2:c.4760_4761del	ENSP00000500665.2:p.Arg1587IlefsTer6
ENST00000674971.1:c.4760_4761del	ENSP00000502194.1:p.Arg1587IlefsTer6
ENST00000675230.1:c.4739_4740del	ENSP00000502503.1:p.Arg1580IlefsTer6
ENST00000675408.1:c.4760_4761del	ENSP00000502298.1:p.Arg1587IlefsTer6
ENST00000675476.1:c.5621_5622del	ENSP00000502161.1:p.Arg1874IlefsTer6
ENST00000675628.1:n.4987_4988del
ENST00000675794.1:c.*2931_*2932del	ENSP00000502841.1:n.*2931_*2932del
ENST00000675833.1:c.5528_5529del	ENSP00000502559.1:p.Arg1843IlefsTer6
ENST00000675894.1:n.1065_1066del
ENST00000676074.1:c.4760_4761del	ENSP00000502079.1:p.Arg1587IlefsTer6
ENST00000676181.1:n.3688_3689del
ENST00000676363.1:n.10486_10487del
ENST00000676448.1:c.*2673_*2674del	ENSP00000501987.1:n.*2673_*2674del
ENST00000309041.11:c.4766_4767del	ENSP00000308021.7:p.Arg1589IlefsTer6
ENST00000547691.6:c.1940_1941del	ENSP00000446905.1:p.Arg647IlefsTer6
ENST00000552810.5:c.4760_4761del	ENSP00000448012.1:p.Arg1587IlefsTer6
NM_025114.3:c.4760_4761del	NP_079390.3:p.Arg1587IlefsTer6
XM_011538756.1:c.5621_5622del	XP_011537058.1:p.Arg1874IlefsTer6
XM_011538757.1:c.5621_5622del	XP_011537059.1:p.Arg1874IlefsTer6
XM_011538758.1:c.5621_5622del	XP_011537060.1:p.Arg1874IlefsTer6
XM_011538759.1:c.5621_5622del	XP_011537061.1:p.Arg1874IlefsTer6
XM_011538760.1:c.5621_5622del	XP_011537062.1:p.Arg1874IlefsTer6
XM_011538761.1:c.5621_5622del	XP_011537063.1:p.Arg1874IlefsTer6
XM_011538762.1:c.4853_4854del	XP_011537064.1:p.Arg1618IlefsTer6
XM_011538763.1:c.4760_4761del	XP_011537065.1:p.Arg1587IlefsTer6
XM_011538764.1:c.5621_5622del	XP_011537066.1:p.Arg1874IlefsTer6
XM_011538765.1:c.5621_5622del	XP_011537067.1:p.Arg1874IlefsTer6
XM_011538766.1:c.4082_4083del	XP_011537068.1:p.Arg1361IlefsTer6
XM_011538756.3:c.5621_5622del	XP_011537058.1:p.Arg1874IlefsTer6
XM_011538757.3:c.5621_5622del	XP_011537059.1:p.Arg1874IlefsTer6
XM_011538758.3:c.5621_5622del	XP_011537060.1:p.Arg1874IlefsTer6
XM_011538759.2:c.5621_5622del	XP_011537061.1:p.Arg1874IlefsTer6
XM_011538760.2:c.5621_5622del	XP_011537062.1:p.Arg1874IlefsTer6
XM_011538761.2:c.5621_5622del	XP_011537063.1:p.Arg1874IlefsTer6
XM_011538762.3:c.4853_4854del	XP_011537064.1:p.Arg1618IlefsTer6
XM_011538763.3:c.4760_4761del	XP_011537065.1:p.Arg1587IlefsTer6
XM_011538764.3:c.5621_5622del	XP_011537066.1:p.Arg1874IlefsTer6
XM_011538765.3:c.5621_5622del	XP_011537067.1:p.Arg1874IlefsTer6
XM_011538766.3:c.4082_4083del	XP_011537068.1:p.Arg1361IlefsTer6
XM_017019980.2:c.5621_5622del	XP_016875469.1:p.Arg1874IlefsTer6
XM_017019981.2:c.5621_5622del	XP_016875470.1:p.Arg1874IlefsTer6
XM_017019982.1:c.5621_5622del	XP_016875471.1:p.Arg1874IlefsTer6
XM_017019983.2:c.4739_4740del	XP_016875472.1:p.Arg1580IlefsTer6
XR_001748869.1:n.5965_5966del
XR_001748870.2:n.5965_5966del
NM_025114.4:c.4760_4761del MANE Select	NP_079390.3:p.Arg1587IlefsTer6