Canonical Allele Identifier: CA481077056

Gene: CEP290

Linked Data

• gnomAD v4: 12-88089413-A-G
• MyVariant Identifiers: chr12:g.88483190A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.88089413A>G , CM000674.2:g.88089413A>G	GRCh38
NC_000012.11:g.88483190A>G , CM000674.1:g.88483190A>G	GRCh37
NC_000012.10:g.87007321A>G	NCBI36
NG_008417.1:g.57804T>C
NG_008417.2:g.57804T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000309041.12:c.3648T>C	ENSP00000308021.8:p.Thr1216=
ENST00000547691.8:c.932T>C
ENST00000552810.6:c.3648T>C MANE Select	ENSP00000448012.1:p.Thr1216=
ENST00000672414.2:c.*1819T>C	ENSP00000500729.1:n.*1819T>C
ENST00000672647.1:n.2008T>C
ENST00000673058.2:c.3648T>C	ENSP00000500665.2:p.Thr1216=
ENST00000674971.1:c.3648T>C	ENSP00000502194.1:p.Thr1216=
ENST00000675089.1:c.473T>C	ENSP00000501582.1:n.473T>C
ENST00000675230.1:c.3627T>C	ENSP00000502503.1:p.Thr1209=
ENST00000675408.1:c.3648T>C	ENSP00000502298.1:p.Thr1216=
ENST00000675476.1:c.4509T>C	ENSP00000502161.1:p.Thr1503=
ENST00000675628.1:n.3875T>C
ENST00000675794.1:c.*1819T>C	ENSP00000502841.1:n.*1819T>C
ENST00000675833.1:c.4416T>C	ENSP00000502559.1:p.Thr1472=
ENST00000676074.1:c.3648T>C	ENSP00000502079.1:p.Thr1216=
ENST00000676181.1:n.2576T>C
ENST00000676363.1:n.9374T>C
ENST00000676448.1:c.*1561T>C	ENSP00000501987.1:n.*1561T>C
ENST00000309041.11:c.3654T>C	ENSP00000308021.7:p.Thr1218=
ENST00000547691.6:c.828T>C	ENSP00000446905.1:p.Thr276=
ENST00000552810.5:c.3648T>C	ENSP00000448012.1:p.Thr1216=
NM_025114.3:c.3648T>C	NP_079390.3:p.Thr1216=
XM_011538756.1:c.4509T>C	XP_011537058.1:p.Thr1503=
XM_011538757.1:c.4509T>C	XP_011537059.1:p.Thr1503=
XM_011538758.1:c.4509T>C	XP_011537060.1:p.Thr1503=
XM_011538759.1:c.4509T>C	XP_011537061.1:p.Thr1503=
XM_011538760.1:c.4509T>C	XP_011537062.1:p.Thr1503=
XM_011538761.1:c.4509T>C	XP_011537063.1:p.Thr1503=
XM_011538762.1:c.3741T>C	XP_011537064.1:p.Thr1247=
XM_011538763.1:c.3648T>C	XP_011537065.1:p.Thr1216=
XM_011538764.1:c.4509T>C	XP_011537066.1:p.Thr1503=
XM_011538765.1:c.4509T>C	XP_011537067.1:p.Thr1503=
XM_011538766.1:c.2970T>C	XP_011537068.1:p.Thr990=
XM_011538756.3:c.4509T>C	XP_011537058.1:p.Thr1503=
XM_011538757.3:c.4509T>C	XP_011537059.1:p.Thr1503=
XM_011538758.3:c.4509T>C	XP_011537060.1:p.Thr1503=
XM_011538759.2:c.4509T>C	XP_011537061.1:p.Thr1503=
XM_011538760.2:c.4509T>C	XP_011537062.1:p.Thr1503=
XM_011538761.2:c.4509T>C	XP_011537063.1:p.Thr1503=
XM_011538762.3:c.3741T>C	XP_011537064.1:p.Thr1247=
XM_011538763.3:c.3648T>C	XP_011537065.1:p.Thr1216=
XM_011538764.3:c.4509T>C	XP_011537066.1:p.Thr1503=
XM_011538765.3:c.4509T>C	XP_011537067.1:p.Thr1503=
XM_011538766.3:c.2970T>C	XP_011537068.1:p.Thr990=
XM_017019980.2:c.4509T>C	XP_016875469.1:p.Thr1503=
XM_017019981.2:c.4509T>C	XP_016875470.1:p.Thr1503=
XM_017019982.1:c.4509T>C	XP_016875471.1:p.Thr1503=
XM_017019983.2:c.3627T>C	XP_016875472.1:p.Thr1209=
XR_001748869.1:n.4853T>C
XR_001748870.2:n.4853T>C
NM_025114.4:c.3648T>C MANE Select	NP_079390.3:p.Thr1216=