Canonical Allele Identifier: CA16043473

Gene: CEP290

Linked Data

• ClinVar Variation Id: 373994
• ClinVar RCV Id: RCV000415004 ; RCV000414899 ; RCV001199375 ; RCV003470364 ; RCV003766165
• dbSNP Id: rs1057518822
• gnomAD v4: 12-88102888-G-A
• MyVariant Identifiers: chr12:g.88496665G>A (hg19) ; chr12:g.88102888G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.88102888G>A , CM000674.2:g.88102888G>A	GRCh38
NC_000012.11:g.88496665G>A , CM000674.1:g.88496665G>A	GRCh37
NC_000012.10:g.87020796G>A	NCBI36
NG_008417.1:g.44329C>T
NG_008417.2:g.44329C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000309041.12:c.2941C>T	ENSP00000308021.8:p.Gln981Ter
ENST00000547691.8:c.225C>T
ENST00000552810.6:c.2941C>T MANE Select	ENSP00000448012.1:p.Gln981Ter
ENST00000672414.2:c.*1112C>T	ENSP00000500729.1:n.*1112C>T
ENST00000672647.1:n.1301C>T
ENST00000673058.2:c.2941C>T	ENSP00000500665.2:p.Gln981Ter
ENST00000674971.1:c.2941C>T	ENSP00000502194.1:p.Gln981Ter
ENST00000675089.1:c.124C>T	ENSP00000501582.1:p.Gln42Ter
ENST00000675230.1:c.2920C>T	ENSP00000502503.1:p.Gln974Ter
ENST00000675408.1:c.2941C>T	ENSP00000502298.1:p.Gln981Ter
ENST00000675476.1:c.3802C>T	ENSP00000502161.1:p.Gln1268Ter
ENST00000675628.1:n.3168C>T
ENST00000675794.1:c.*1112C>T	ENSP00000502841.1:n.*1112C>T
ENST00000675833.1:c.3709C>T	ENSP00000502559.1:p.Gln1237Ter
ENST00000676074.1:c.2941C>T	ENSP00000502079.1:p.Gln981Ter
ENST00000676181.1:n.629C>T
ENST00000676363.1:n.8667C>T
ENST00000676448.1:c.*854C>T	ENSP00000501987.1:n.*854C>T
ENST00000309041.11:c.2947C>T	ENSP00000308021.7:p.Gln983Ter
ENST00000547691.6:c.121C>T	ENSP00000446905.1:p.Gln41Ter
ENST00000552810.5:c.2941C>T	ENSP00000448012.1:p.Gln981Ter
ENST00000604024.5:c.2200C>T	ENSP00000473863.1:p.Gln734Ter
NM_025114.3:c.2941C>T	NP_079390.3:p.Gln981Ter
XM_011538756.1:c.3802C>T	XP_011537058.1:p.Gln1268Ter
XM_011538757.1:c.3802C>T	XP_011537059.1:p.Gln1268Ter
XM_011538758.1:c.3802C>T	XP_011537060.1:p.Gln1268Ter
XM_011538759.1:c.3802C>T	XP_011537061.1:p.Gln1268Ter
XM_011538760.1:c.3802C>T	XP_011537062.1:p.Gln1268Ter
XM_011538761.1:c.3802C>T	XP_011537063.1:p.Gln1268Ter
XM_011538762.1:c.3034C>T	XP_011537064.1:p.Gln1012Ter
XM_011538763.1:c.2941C>T	XP_011537065.1:p.Gln981Ter
XM_011538764.1:c.3802C>T	XP_011537066.1:p.Gln1268Ter
XM_011538765.1:c.3802C>T	XP_011537067.1:p.Gln1268Ter
XM_011538766.1:c.2263C>T	XP_011537068.1:p.Gln755Ter
XM_011538756.3:c.3802C>T	XP_011537058.1:p.Gln1268Ter
XM_011538757.3:c.3802C>T	XP_011537059.1:p.Gln1268Ter
XM_011538758.3:c.3802C>T	XP_011537060.1:p.Gln1268Ter
XM_011538759.2:c.3802C>T	XP_011537061.1:p.Gln1268Ter
XM_011538760.2:c.3802C>T	XP_011537062.1:p.Gln1268Ter
XM_011538761.2:c.3802C>T	XP_011537063.1:p.Gln1268Ter
XM_011538762.3:c.3034C>T	XP_011537064.1:p.Gln1012Ter
XM_011538763.3:c.2941C>T	XP_011537065.1:p.Gln981Ter
XM_011538764.3:c.3802C>T	XP_011537066.1:p.Gln1268Ter
XM_011538765.3:c.3802C>T	XP_011537067.1:p.Gln1268Ter
XM_011538766.3:c.2263C>T	XP_011537068.1:p.Gln755Ter
XM_017019980.2:c.3802C>T	XP_016875469.1:p.Gln1268Ter
XM_017019981.2:c.3802C>T	XP_016875470.1:p.Gln1268Ter
XM_017019982.1:c.3802C>T	XP_016875471.1:p.Gln1268Ter
XM_017019983.2:c.2920C>T	XP_016875472.1:p.Gln974Ter
XR_001748869.1:n.4146C>T
XR_001748870.2:n.4146C>T
NM_025114.4:c.2941C>T MANE Select	NP_079390.3:p.Gln981Ter