Canonical Allele Identifier: CA2052913813

Gene: CEP290

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.88077316_88077317delinsCT , CM000674.2:g.88077316_88077317delinsCT	GRCh38
NC_000012.11:g.88471093_88471094delinsCT , CM000674.1:g.88471093_88471094delinsCT	GRCh37
NC_000012.10:g.86995224_86995225delinsCT	NCBI36
NG_008417.1:g.69900_69901delinsAG
NG_008417.2:g.69900_69901delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000309041.12:c.5614_5615delinsAG	ENSP00000308021.8:p.Ser1872=
ENST00000547691.8:c.2898_2899delinsAG
ENST00000552810.6:c.5614_5615delinsAG MANE Select	ENSP00000448012.1:p.Ser1872=
ENST00000672414.2:c.*3785_*3786delinsAG	ENSP00000500729.1:n.*3785_*3786delinsAG
ENST00000672647.1:n.3974_3975delinsAG
ENST00000673058.2:c.5614_5615delinsAG	ENSP00000500665.2:p.Ser1872=
ENST00000674971.1:c.5614_5615delinsAG	ENSP00000502194.1:p.Ser1872=
ENST00000675230.1:c.5593_5594delinsAG	ENSP00000502503.1:p.Ser1865=
ENST00000675408.1:c.5614_5615delinsAG	ENSP00000502298.1:p.Ser1872=
ENST00000675476.1:c.6475_6476delinsAG	ENSP00000502161.1:p.Ser2159=
ENST00000675628.1:n.5841_5842delinsAG
ENST00000675794.1:c.*3785_*3786delinsAG	ENSP00000502841.1:n.*3785_*3786delinsAG
ENST00000675833.1:c.6382_6383delinsAG	ENSP00000502559.1:p.Ser2128=
ENST00000675894.1:n.1919_1920delinsAG
ENST00000676074.1:c.5614_5615delinsAG	ENSP00000502079.1:p.Ser1872=
ENST00000676181.1:n.4542_4543delinsAG
ENST00000676363.1:n.11340_11341delinsAG
ENST00000676448.1:c.*3527_*3528delinsAG	ENSP00000501987.1:n.*3527_*3528delinsAG
ENST00000309041.11:c.5620_5621delinsAG	ENSP00000308021.7:p.Ser1874=
ENST00000547691.6:c.2794_2795delinsAG	ENSP00000446905.1:p.Ser932=
ENST00000552810.5:c.5614_5615delinsAG	ENSP00000448012.1:p.Ser1872=
NM_025114.3:c.5614_5615delinsAG	NP_079390.3:p.Ser1872=
XM_011538756.1:c.6475_6476delinsAG	XP_011537058.1:p.Ser2159=
XM_011538757.1:c.6475_6476delinsAG	XP_011537059.1:p.Ser2159=
XM_011538758.1:c.6475_6476delinsAG	XP_011537060.1:p.Ser2159=
XM_011538759.1:c.6475_6476delinsAG	XP_011537061.1:p.Ser2159=
XM_011538760.1:c.6475_6476delinsAG	XP_011537062.1:p.Ser2159=
XM_011538761.1:c.6475_6476delinsAG	XP_011537063.1:p.Ser2159=
XM_011538762.1:c.5707_5708delinsAG	XP_011537064.1:p.Ser1903=
XM_011538763.1:c.5614_5615delinsAG	XP_011537065.1:p.Ser1872=
XM_011538764.1:c.6475_6476delinsAG	XP_011537066.1:p.Ser2159=
XM_011538765.1:c.6475_6476delinsAG	XP_011537067.1:p.Ser2159=
XM_011538766.1:c.4936_4937delinsAG	XP_011537068.1:p.Ser1646=
XR_945163.1:n.968-4997_968-4996delinsCT
XM_011538756.3:c.6475_6476delinsAG	XP_011537058.1:p.Ser2159=
XM_011538757.3:c.6475_6476delinsAG	XP_011537059.1:p.Ser2159=
XM_011538758.3:c.6475_6476delinsAG	XP_011537060.1:p.Ser2159=
XM_011538759.2:c.6475_6476delinsAG	XP_011537061.1:p.Ser2159=
XM_011538760.2:c.6475_6476delinsAG	XP_011537062.1:p.Ser2159=
XM_011538761.2:c.6475_6476delinsAG	XP_011537063.1:p.Ser2159=
XM_011538762.3:c.5707_5708delinsAG	XP_011537064.1:p.Ser1903=
XM_011538763.3:c.5614_5615delinsAG	XP_011537065.1:p.Ser1872=
XM_011538764.3:c.6475_6476delinsAG	XP_011537066.1:p.Ser2159=
XM_011538765.3:c.6475_6476delinsAG	XP_011537067.1:p.Ser2159=
XM_011538766.3:c.4936_4937delinsAG	XP_011537068.1:p.Ser1646=
XM_017019980.2:c.6475_6476delinsAG	XP_016875469.1:p.Ser2159=
XM_017019981.2:c.6475_6476delinsAG	XP_016875470.1:p.Ser2159=
XM_017019982.1:c.6475_6476delinsAG	XP_016875471.1:p.Ser2159=
XM_017019983.2:c.5593_5594delinsAG	XP_016875472.1:p.Ser1865=
XR_001748869.1:n.6819_6820delinsAG
XR_001748870.2:n.6819_6820delinsAG
NM_025114.4:c.5614_5615delinsAG MANE Select	NP_079390.3:p.Ser1872=