Canonical Allele Identifier: CA386007296

Gene: CEP290

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.88097001T>G , CM000674.2:g.88097001T>G	GRCh38
NC_000012.11:g.88490778T>G , CM000674.1:g.88490778T>G	GRCh37
NC_000012.10:g.87014909T>G	NCBI36
NG_008417.1:g.50216A>C
NG_008417.2:g.50216A>C

Transcript Alleles

HGVS	Amino-acid Change
NM_025114.4:c.2992-2A>C MANE Select	NP_079390.3:n.2992-2A>C
ENST00000552810.6:c.2992-2A>C MANE Select	ENSP00000448012.1:n.2992-2A>C
NM_025114.3:c.2992-2A>C	NP_079390.3:n.2992-2A>C
ENST00000309041.11:c.2998-2A>C	ENSP00000308021.7:n.2998-2A>C
ENST00000309041.12:c.2992-2A>C	ENSP00000308021.8:n.2992-2A>C
ENST00000547691.6:c.172-2A>C	ENSP00000446905.1:n.172-2A>C
ENST00000547691.8:c.276-2A>C
ENST00000552810.5:c.2992-2A>C	ENSP00000448012.1:n.2992-2A>C
ENST00000604024.5:c.2251-2A>C	ENSP00000473863.1:n.2251-2A>C
ENST00000672414.2:c.*1163-2A>C	ENSP00000500729.1:n.*1163-2A>C
ENST00000672647.1:n.1352-2A>C
ENST00000673058.2:c.2992-2A>C	ENSP00000500665.2:n.2992-2A>C
ENST00000674971.1:c.2992-2A>C	ENSP00000502194.1:n.2992-2A>C
ENST00000675089.1:c.175-2A>C	ENSP00000501582.1:n.175-2A>C
ENST00000675230.1:c.2971-2A>C	ENSP00000502503.1:n.2971-2A>C
ENST00000675408.1:c.2992-2A>C	ENSP00000502298.1:n.2992-2A>C
ENST00000675476.1:c.3853-2A>C	ENSP00000502161.1:n.3853-2A>C
ENST00000675628.1:n.3219-2A>C
ENST00000675794.1:c.*1163-2A>C	ENSP00000502841.1:n.*1163-2A>C
ENST00000675833.1:c.3760-2A>C	ENSP00000502559.1:n.3760-2A>C
ENST00000676074.1:c.2992-2A>C	ENSP00000502079.1:n.2992-2A>C
ENST00000676181.1:n.680-2A>C
ENST00000676363.1:n.8718-2A>C
ENST00000676448.1:c.*905-2A>C	ENSP00000501987.1:n.*905-2A>C
XM_011538756.1:c.3853-2A>C	XP_011537058.1:n.3853-2A>C
XM_011538756.3:c.3853-2A>C	XP_011537058.1:n.3853-2A>C
XM_011538757.1:c.3853-2A>C	XP_011537059.1:n.3853-2A>C
XM_011538757.3:c.3853-2A>C	XP_011537059.1:n.3853-2A>C
XM_011538758.1:c.3853-2A>C	XP_011537060.1:n.3853-2A>C
XM_011538758.3:c.3853-2A>C	XP_011537060.1:n.3853-2A>C
XM_011538759.1:c.3853-2A>C	XP_011537061.1:n.3853-2A>C
XM_011538759.2:c.3853-2A>C	XP_011537061.1:n.3853-2A>C
XM_011538760.1:c.3853-2A>C	XP_011537062.1:n.3853-2A>C
XM_011538760.2:c.3853-2A>C	XP_011537062.1:n.3853-2A>C
XM_011538761.1:c.3853-2A>C	XP_011537063.1:n.3853-2A>C
XM_011538761.2:c.3853-2A>C	XP_011537063.1:n.3853-2A>C
XM_011538762.1:c.3085-2A>C	XP_011537064.1:n.3085-2A>C
XM_011538762.3:c.3085-2A>C	XP_011537064.1:n.3085-2A>C
XM_011538763.1:c.2992-2A>C	XP_011537065.1:n.2992-2A>C
XM_011538763.3:c.2992-2A>C	XP_011537065.1:n.2992-2A>C
XM_011538764.1:c.3853-2A>C	XP_011537066.1:n.3853-2A>C
XM_011538764.3:c.3853-2A>C	XP_011537066.1:n.3853-2A>C
XM_011538765.1:c.3853-2A>C	XP_011537067.1:n.3853-2A>C
XM_011538765.3:c.3853-2A>C	XP_011537067.1:n.3853-2A>C
XM_011538766.1:c.2314-2A>C	XP_011537068.1:n.2314-2A>C
XM_011538766.3:c.2314-2A>C	XP_011537068.1:n.2314-2A>C
XM_017019980.2:c.3853-2A>C	XP_016875469.1:n.3853-2A>C
XM_017019981.2:c.3853-2A>C	XP_016875470.1:n.3853-2A>C
XM_017019982.1:c.3853-2A>C	XP_016875471.1:n.3853-2A>C
XM_017019983.2:c.2971-2A>C	XP_016875472.1:n.2971-2A>C
XR_001748869.1:n.4197-2A>C
XR_001748870.2:n.4197-2A>C