Canonical Allele Identifier: CA2052905047

Gene: CEP290

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.88083845_88083846delinsAC , CM000674.2:g.88083845_88083846delinsAC	GRCh38
NC_000012.11:g.88477622_88477623delinsAC , CM000674.1:g.88477622_88477623delinsAC	GRCh37
NC_000012.10:g.87001753_87001754delinsAC	NCBI36
NG_008417.1:g.63371_63372delinsGT
NG_008417.2:g.63371_63372delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000309041.12:c.4812+1_4812+2delinsGT	ENSP00000308021.8:n.4812+1_4812+2delinsGT
ENST00000547691.8:c.2096+1_2096+2delinsGT
ENST00000552810.6:c.4812+1_4812+2delinsGT MANE Select	ENSP00000448012.1:n.4812+1_4812+2delinsGT
ENST00000672414.2:c.*2983+1_*2983+2delinsGT	ENSP00000500729.1:n.*2983+1_*2983+2delinsGT
ENST00000672647.1:n.3172+1_3172+2delinsGT
ENST00000673058.2:c.4812+1_4812+2delinsGT	ENSP00000500665.2:n.4812+1_4812+2delinsGT
ENST00000674971.1:c.4812+1_4812+2delinsGT	ENSP00000502194.1:n.4812+1_4812+2delinsGT
ENST00000675230.1:c.4791+1_4791+2delinsGT	ENSP00000502503.1:n.4791+1_4791+2delinsGT
ENST00000675408.1:c.4812+1_4812+2delinsGT	ENSP00000502298.1:n.4812+1_4812+2delinsGT
ENST00000675476.1:c.5673+1_5673+2delinsGT	ENSP00000502161.1:n.5673+1_5673+2delinsGT
ENST00000675628.1:n.5039+1_5039+2delinsGT
ENST00000675794.1:c.*2983+1_*2983+2delinsGT	ENSP00000502841.1:n.*2983+1_*2983+2delinsGT
ENST00000675833.1:c.5580+1_5580+2delinsGT	ENSP00000502559.1:n.5580+1_5580+2delinsGT
ENST00000675894.1:n.1117+1_1117+2delinsGT
ENST00000676074.1:c.4812+1_4812+2delinsGT	ENSP00000502079.1:n.4812+1_4812+2delinsGT
ENST00000676181.1:n.3740+1_3740+2delinsGT
ENST00000676363.1:n.10538+1_10538+2delinsGT
ENST00000676448.1:c.*2725+1_*2725+2delinsGT	ENSP00000501987.1:n.*2725+1_*2725+2delinsGT
ENST00000309041.11:c.4818+1_4818+2delinsGT	ENSP00000308021.7:n.4818+1_4818+2delinsGT
ENST00000547691.6:c.1992+1_1992+2delinsGT	ENSP00000446905.1:n.1992+1_1992+2delinsGT
ENST00000552810.5:c.4812+1_4812+2delinsGT	ENSP00000448012.1:n.4812+1_4812+2delinsGT
NM_025114.3:c.4812+1_4812+2delinsGT	NP_079390.3:n.4812+1_4812+2delinsGT
XM_011538756.1:c.5673+1_5673+2delinsGT	XP_011537058.1:n.5673+1_5673+2delinsGT
XM_011538757.1:c.5673+1_5673+2delinsGT	XP_011537059.1:n.5673+1_5673+2delinsGT
XM_011538758.1:c.5673+1_5673+2delinsGT	XP_011537060.1:n.5673+1_5673+2delinsGT
XM_011538759.1:c.5673+1_5673+2delinsGT	XP_011537061.1:n.5673+1_5673+2delinsGT
XM_011538760.1:c.5673+1_5673+2delinsGT	XP_011537062.1:n.5673+1_5673+2delinsGT
XM_011538761.1:c.5673+1_5673+2delinsGT	XP_011537063.1:n.5673+1_5673+2delinsGT
XM_011538762.1:c.4905+1_4905+2delinsGT	XP_011537064.1:n.4905+1_4905+2delinsGT
XM_011538763.1:c.4812+1_4812+2delinsGT	XP_011537065.1:n.4812+1_4812+2delinsGT
XM_011538764.1:c.5673+1_5673+2delinsGT	XP_011537066.1:n.5673+1_5673+2delinsGT
XM_011538765.1:c.5673+1_5673+2delinsGT	XP_011537067.1:n.5673+1_5673+2delinsGT
XM_011538766.1:c.4134+1_4134+2delinsGT	XP_011537068.1:n.4134+1_4134+2delinsGT
XM_011538756.3:c.5673+1_5673+2delinsGT	XP_011537058.1:n.5673+1_5673+2delinsGT
XM_011538757.3:c.5673+1_5673+2delinsGT	XP_011537059.1:n.5673+1_5673+2delinsGT
XM_011538758.3:c.5673+1_5673+2delinsGT	XP_011537060.1:n.5673+1_5673+2delinsGT
XM_011538759.2:c.5673+1_5673+2delinsGT	XP_011537061.1:n.5673+1_5673+2delinsGT
XM_011538760.2:c.5673+1_5673+2delinsGT	XP_011537062.1:n.5673+1_5673+2delinsGT
XM_011538761.2:c.5673+1_5673+2delinsGT	XP_011537063.1:n.5673+1_5673+2delinsGT
XM_011538762.3:c.4905+1_4905+2delinsGT	XP_011537064.1:n.4905+1_4905+2delinsGT
XM_011538763.3:c.4812+1_4812+2delinsGT	XP_011537065.1:n.4812+1_4812+2delinsGT
XM_011538764.3:c.5673+1_5673+2delinsGT	XP_011537066.1:n.5673+1_5673+2delinsGT
XM_011538765.3:c.5673+1_5673+2delinsGT	XP_011537067.1:n.5673+1_5673+2delinsGT
XM_011538766.3:c.4134+1_4134+2delinsGT	XP_011537068.1:n.4134+1_4134+2delinsGT
XM_017019980.2:c.5673+1_5673+2delinsGT	XP_016875469.1:n.5673+1_5673+2delinsGT
XM_017019981.2:c.5673+1_5673+2delinsGT	XP_016875470.1:n.5673+1_5673+2delinsGT
XM_017019982.1:c.5673+1_5673+2delinsGT	XP_016875471.1:n.5673+1_5673+2delinsGT
XM_017019983.2:c.4791+1_4791+2delinsGT	XP_016875472.1:n.4791+1_4791+2delinsGT
XR_001748869.1:n.6017+1_6017+2delinsGT
XR_001748870.2:n.6017+1_6017+2delinsGT
NM_025114.4:c.4812+1_4812+2delinsGT MANE Select	NP_079390.3:n.4812+1_4812+2delinsGT