Canonical Allele Identifier: CA10606630

Gene: CEP290

Linked Data

• ClinVar Variation Id: 290022
• ClinVar RCV Id: RCV000268793 ; RCV001859707
• dbSNP Id: rs886044332
• gnomAD v4: 12-88106824-G-A
• MyVariant Identifiers: chr12:g.88500601G>A (hg19) ; chr12:g.88106824G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.88106824G>A , CM000674.2:g.88106824G>A	GRCh38
NC_000012.11:g.88500601G>A , CM000674.1:g.88500601G>A	GRCh37
NC_000012.10:g.87024732G>A	NCBI36
NG_008417.1:g.40393C>T
NG_008417.2:g.40393C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000309041.12:c.2668C>T	ENSP00000308021.8:p.Gln890Ter
ENST00000552810.6:c.2668C>T MANE Select	ENSP00000448012.1:p.Gln890Ter
ENST00000672414.2:c.*839C>T	ENSP00000500729.1:n.*839C>T
ENST00000673058.2:c.2668C>T	ENSP00000500665.2:p.Gln890Ter
ENST00000674971.1:c.2668C>T	ENSP00000502194.1:p.Gln890Ter
ENST00000675230.1:c.2647C>T	ENSP00000502503.1:p.Gln883Ter
ENST00000675408.1:c.2668C>T	ENSP00000502298.1:p.Gln890Ter
ENST00000675476.1:c.3529C>T	ENSP00000502161.1:p.Gln1177Ter
ENST00000675628.1:n.2895C>T
ENST00000675794.1:c.*839C>T	ENSP00000502841.1:n.*839C>T
ENST00000675833.1:c.3436C>T	ENSP00000502559.1:p.Gln1146Ter
ENST00000676074.1:c.2668C>T	ENSP00000502079.1:p.Gln890Ter
ENST00000676363.1:n.4731C>T
ENST00000676448.1:c.*581C>T	ENSP00000501987.1:n.*581C>T
ENST00000309041.11:c.2674C>T	ENSP00000308021.7:p.Gln892Ter
ENST00000552810.5:c.2668C>T	ENSP00000448012.1:p.Gln890Ter
ENST00000604024.5:c.1927C>T	ENSP00000473863.1:p.Gln643Ter
NM_025114.3:c.2668C>T	NP_079390.3:p.Gln890Ter
XM_011538756.1:c.3529C>T	XP_011537058.1:p.Gln1177Ter
XM_011538757.1:c.3529C>T	XP_011537059.1:p.Gln1177Ter
XM_011538758.1:c.3529C>T	XP_011537060.1:p.Gln1177Ter
XM_011538759.1:c.3529C>T	XP_011537061.1:p.Gln1177Ter
XM_011538760.1:c.3529C>T	XP_011537062.1:p.Gln1177Ter
XM_011538761.1:c.3529C>T	XP_011537063.1:p.Gln1177Ter
XM_011538762.1:c.2761C>T	XP_011537064.1:p.Gln921Ter
XM_011538763.1:c.2668C>T	XP_011537065.1:p.Gln890Ter
XM_011538764.1:c.3529C>T	XP_011537066.1:p.Gln1177Ter
XM_011538765.1:c.3529C>T	XP_011537067.1:p.Gln1177Ter
XM_011538766.1:c.1990C>T	XP_011537068.1:p.Gln664Ter
XM_011538756.3:c.3529C>T	XP_011537058.1:p.Gln1177Ter
XM_011538757.3:c.3529C>T	XP_011537059.1:p.Gln1177Ter
XM_011538758.3:c.3529C>T	XP_011537060.1:p.Gln1177Ter
XM_011538759.2:c.3529C>T	XP_011537061.1:p.Gln1177Ter
XM_011538760.2:c.3529C>T	XP_011537062.1:p.Gln1177Ter
XM_011538761.2:c.3529C>T	XP_011537063.1:p.Gln1177Ter
XM_011538762.3:c.2761C>T	XP_011537064.1:p.Gln921Ter
XM_011538763.3:c.2668C>T	XP_011537065.1:p.Gln890Ter
XM_011538764.3:c.3529C>T	XP_011537066.1:p.Gln1177Ter
XM_011538765.3:c.3529C>T	XP_011537067.1:p.Gln1177Ter
XM_011538766.3:c.1990C>T	XP_011537068.1:p.Gln664Ter
XM_017019980.2:c.3529C>T	XP_016875469.1:p.Gln1177Ter
XM_017019981.2:c.3529C>T	XP_016875470.1:p.Gln1177Ter
XM_017019982.1:c.3529C>T	XP_016875471.1:p.Gln1177Ter
XM_017019983.2:c.2647C>T	XP_016875472.1:p.Gln883Ter
XR_001748869.1:n.3873C>T
XR_001748870.2:n.3873C>T
NM_025114.4:c.2668C>T MANE Select	NP_079390.3:p.Gln890Ter