Canonical Allele Identifier: CA6711837

Gene: CEP290

Linked Data

• ClinVar Variation Id: 1696401
• ClinVar RCV Id: RCV002266546 ; RCV002488667 ; RCV003101514
• dbSNP Id: rs758453972
• ExAC: 12:88476955 C / T
• gnomAD v2: 12-88476955-C-T
• gnomAD v3: 12-88083178-C-T
• gnomAD v4: 12-88083178-C-T
• MyVariant Identifiers: chr12:g.88476955C>T (hg19) ; chr12:g.88083178C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.88083178C>T , CM000674.2:g.88083178C>T	GRCh38
NC_000012.11:g.88476955C>T , CM000674.1:g.88476955C>T	GRCh37
NC_000012.10:g.87001086C>T	NCBI36
NG_008417.1:g.64039G>A
NG_008417.2:g.64039G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000309041.12:c.4865G>A	ENSP00000308021.8:p.Arg1622His
ENST00000547691.8:c.2149G>A
ENST00000552810.6:c.4865G>A MANE Select	ENSP00000448012.1:p.Arg1622His
ENST00000672414.2:c.*3036G>A	ENSP00000500729.1:n.*3036G>A
ENST00000672647.1:n.3225G>A
ENST00000673058.2:c.4865G>A	ENSP00000500665.2:p.Arg1622His
ENST00000674971.1:c.4865G>A	ENSP00000502194.1:p.Arg1622His
ENST00000675230.1:c.4844G>A	ENSP00000502503.1:p.Arg1615His
ENST00000675408.1:c.4865G>A	ENSP00000502298.1:p.Arg1622His
ENST00000675476.1:c.5726G>A	ENSP00000502161.1:p.Arg1909His
ENST00000675628.1:n.5092G>A
ENST00000675794.1:c.*3036G>A	ENSP00000502841.1:n.*3036G>A
ENST00000675833.1:c.5633G>A	ENSP00000502559.1:p.Arg1878His
ENST00000675894.1:n.1170G>A
ENST00000676074.1:c.4865G>A	ENSP00000502079.1:p.Arg1622His
ENST00000676181.1:n.3793G>A
ENST00000676363.1:n.10591G>A
ENST00000676448.1:c.*2778G>A	ENSP00000501987.1:n.*2778G>A
ENST00000309041.11:c.4871G>A	ENSP00000308021.7:p.Arg1624His
ENST00000547691.6:c.2045G>A	ENSP00000446905.1:p.Arg682His
ENST00000552810.5:c.4865G>A	ENSP00000448012.1:p.Arg1622His
NM_025114.3:c.4865G>A	NP_079390.3:p.Arg1622His
XM_011538756.1:c.5726G>A	XP_011537058.1:p.Arg1909His
XM_011538757.1:c.5726G>A	XP_011537059.1:p.Arg1909His
XM_011538758.1:c.5726G>A	XP_011537060.1:p.Arg1909His
XM_011538759.1:c.5726G>A	XP_011537061.1:p.Arg1909His
XM_011538760.1:c.5726G>A	XP_011537062.1:p.Arg1909His
XM_011538761.1:c.5726G>A	XP_011537063.1:p.Arg1909His
XM_011538762.1:c.4958G>A	XP_011537064.1:p.Arg1653His
XM_011538763.1:c.4865G>A	XP_011537065.1:p.Arg1622His
XM_011538764.1:c.5726G>A	XP_011537066.1:p.Arg1909His
XM_011538765.1:c.5726G>A	XP_011537067.1:p.Arg1909His
XM_011538766.1:c.4187G>A	XP_011537068.1:p.Arg1396His
XM_011538756.3:c.5726G>A	XP_011537058.1:p.Arg1909His
XM_011538757.3:c.5726G>A	XP_011537059.1:p.Arg1909His
XM_011538758.3:c.5726G>A	XP_011537060.1:p.Arg1909His
XM_011538759.2:c.5726G>A	XP_011537061.1:p.Arg1909His
XM_011538760.2:c.5726G>A	XP_011537062.1:p.Arg1909His
XM_011538761.2:c.5726G>A	XP_011537063.1:p.Arg1909His
XM_011538762.3:c.4958G>A	XP_011537064.1:p.Arg1653His
XM_011538763.3:c.4865G>A	XP_011537065.1:p.Arg1622His
XM_011538764.3:c.5726G>A	XP_011537066.1:p.Arg1909His
XM_011538765.3:c.5726G>A	XP_011537067.1:p.Arg1909His
XM_011538766.3:c.4187G>A	XP_011537068.1:p.Arg1396His
XM_017019980.2:c.5726G>A	XP_016875469.1:p.Arg1909His
XM_017019981.2:c.5726G>A	XP_016875470.1:p.Arg1909His
XM_017019982.1:c.5726G>A	XP_016875471.1:p.Arg1909His
XM_017019983.2:c.4844G>A	XP_016875472.1:p.Arg1615His
XR_001748869.1:n.6070G>A
XR_001748870.2:n.6070G>A
NM_025114.4:c.4865G>A MANE Select	NP_079390.3:p.Arg1622His