Canonical Allele Identifier: CA481076296

Gene: CEP290

Linked Data

• ClinVar Variation Id: 2948864
• ClinVar RCV Id: RCV003809638
• MyVariant Identifiers: chr12:g.88477630C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.88083853C>G , CM000674.2:g.88083853C>G	GRCh38
NC_000012.11:g.88477630C>G , CM000674.1:g.88477630C>G	GRCh37
NC_000012.10:g.87001761C>G	NCBI36
NG_008417.1:g.63364G>C
NG_008417.2:g.63364G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000309041.12:c.4806G>C	ENSP00000308021.8:p.Thr1602=
ENST00000547691.8:c.2090G>C
ENST00000552810.6:c.4806G>C MANE Select	ENSP00000448012.1:p.Thr1602=
ENST00000672414.2:c.*2977G>C	ENSP00000500729.1:n.*2977G>C
ENST00000672647.1:n.3166G>C
ENST00000673058.2:c.4806G>C	ENSP00000500665.2:p.Thr1602=
ENST00000674971.1:c.4806G>C	ENSP00000502194.1:p.Thr1602=
ENST00000675230.1:c.4785G>C	ENSP00000502503.1:p.Thr1595=
ENST00000675408.1:c.4806G>C	ENSP00000502298.1:p.Thr1602=
ENST00000675476.1:c.5667G>C	ENSP00000502161.1:p.Thr1889=
ENST00000675628.1:n.5033G>C
ENST00000675794.1:c.*2977G>C	ENSP00000502841.1:n.*2977G>C
ENST00000675833.1:c.5574G>C	ENSP00000502559.1:p.Thr1858=
ENST00000675894.1:n.1111G>C
ENST00000676074.1:c.4806G>C	ENSP00000502079.1:p.Thr1602=
ENST00000676181.1:n.3734G>C
ENST00000676363.1:n.10532G>C
ENST00000676448.1:c.*2719G>C	ENSP00000501987.1:n.*2719G>C
ENST00000309041.11:c.4812G>C	ENSP00000308021.7:p.Thr1604=
ENST00000547691.6:c.1986G>C	ENSP00000446905.1:p.Thr662=
ENST00000552810.5:c.4806G>C	ENSP00000448012.1:p.Thr1602=
NM_025114.3:c.4806G>C	NP_079390.3:p.Thr1602=
XM_011538756.1:c.5667G>C	XP_011537058.1:p.Thr1889=
XM_011538757.1:c.5667G>C	XP_011537059.1:p.Thr1889=
XM_011538758.1:c.5667G>C	XP_011537060.1:p.Thr1889=
XM_011538759.1:c.5667G>C	XP_011537061.1:p.Thr1889=
XM_011538760.1:c.5667G>C	XP_011537062.1:p.Thr1889=
XM_011538761.1:c.5667G>C	XP_011537063.1:p.Thr1889=
XM_011538762.1:c.4899G>C	XP_011537064.1:p.Thr1633=
XM_011538763.1:c.4806G>C	XP_011537065.1:p.Thr1602=
XM_011538764.1:c.5667G>C	XP_011537066.1:p.Thr1889=
XM_011538765.1:c.5667G>C	XP_011537067.1:p.Thr1889=
XM_011538766.1:c.4128G>C	XP_011537068.1:p.Thr1376=
XM_011538756.3:c.5667G>C	XP_011537058.1:p.Thr1889=
XM_011538757.3:c.5667G>C	XP_011537059.1:p.Thr1889=
XM_011538758.3:c.5667G>C	XP_011537060.1:p.Thr1889=
XM_011538759.2:c.5667G>C	XP_011537061.1:p.Thr1889=
XM_011538760.2:c.5667G>C	XP_011537062.1:p.Thr1889=
XM_011538761.2:c.5667G>C	XP_011537063.1:p.Thr1889=
XM_011538762.3:c.4899G>C	XP_011537064.1:p.Thr1633=
XM_011538763.3:c.4806G>C	XP_011537065.1:p.Thr1602=
XM_011538764.3:c.5667G>C	XP_011537066.1:p.Thr1889=
XM_011538765.3:c.5667G>C	XP_011537067.1:p.Thr1889=
XM_011538766.3:c.4128G>C	XP_011537068.1:p.Thr1376=
XM_017019980.2:c.5667G>C	XP_016875469.1:p.Thr1889=
XM_017019981.2:c.5667G>C	XP_016875470.1:p.Thr1889=
XM_017019982.1:c.5667G>C	XP_016875471.1:p.Thr1889=
XM_017019983.2:c.4785G>C	XP_016875472.1:p.Thr1595=
XR_001748869.1:n.6011G>C
XR_001748870.2:n.6011G>C
NM_025114.4:c.4806G>C MANE Select	NP_079390.3:p.Thr1602=