Canonical Allele Identifier: CA385987305

Gene: CEP290

Linked Data

• MyVariant Identifiers: chr12:g.88471016T>G (hg19) ; chr12:g.88077239T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.88077239T>G , CM000674.2:g.88077239T>G	GRCh38
NC_000012.11:g.88471016T>G , CM000674.1:g.88471016T>G	GRCh37
NC_000012.10:g.86995147T>G	NCBI36
NG_008417.1:g.69978A>C
NG_008417.2:g.69978A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000309041.12:c.5692A>C	ENSP00000308021.8:p.Lys1898Gln
ENST00000547691.8:c.2976A>C
ENST00000552810.6:c.5692A>C MANE Select	ENSP00000448012.1:p.Lys1898Gln
ENST00000672414.2:c.*3863A>C	ENSP00000500729.1:n.*3863A>C
ENST00000672647.1:n.4052A>C
ENST00000673058.2:c.5692A>C	ENSP00000500665.2:p.Lys1898Gln
ENST00000674971.1:c.5692A>C	ENSP00000502194.1:p.Lys1898Gln
ENST00000675230.1:c.5671A>C	ENSP00000502503.1:p.Lys1891Gln
ENST00000675408.1:c.5692A>C	ENSP00000502298.1:p.Lys1898Gln
ENST00000675476.1:c.6553A>C	ENSP00000502161.1:p.Lys2185Gln
ENST00000675628.1:n.5919A>C
ENST00000675794.1:c.*3863A>C	ENSP00000502841.1:n.*3863A>C
ENST00000675833.1:c.6460A>C	ENSP00000502559.1:p.Lys2154Gln
ENST00000675894.1:n.1997A>C
ENST00000676074.1:c.5692A>C	ENSP00000502079.1:p.Lys1898Gln
ENST00000676181.1:n.4620A>C
ENST00000676363.1:n.11418A>C
ENST00000676448.1:c.*3605A>C	ENSP00000501987.1:n.*3605A>C
ENST00000309041.11:c.5698A>C	ENSP00000308021.7:p.Lys1900Gln
ENST00000547691.6:c.2872A>C	ENSP00000446905.1:p.Lys958Gln
ENST00000552810.5:c.5692A>C	ENSP00000448012.1:p.Lys1898Gln
NM_025114.3:c.5692A>C	NP_079390.3:p.Lys1898Gln
XM_011538756.1:c.6553A>C	XP_011537058.1:p.Lys2185Gln
XM_011538757.1:c.6553A>C	XP_011537059.1:p.Lys2185Gln
XM_011538758.1:c.6553A>C	XP_011537060.1:p.Lys2185Gln
XM_011538759.1:c.6553A>C	XP_011537061.1:p.Lys2185Gln
XM_011538760.1:c.6553A>C	XP_011537062.1:p.Lys2185Gln
XM_011538761.1:c.6553A>C	XP_011537063.1:p.Lys2185Gln
XM_011538762.1:c.5785A>C	XP_011537064.1:p.Lys1929Gln
XM_011538763.1:c.5692A>C	XP_011537065.1:p.Lys1898Gln
XM_011538764.1:c.6553A>C	XP_011537066.1:p.Lys2185Gln
XM_011538765.1:c.6553A>C	XP_011537067.1:p.Lys2185Gln
XM_011538766.1:c.5014A>C	XP_011537068.1:p.Lys1672Gln
XR_945163.1:n.968-5074T>G
XM_011538756.3:c.6553A>C	XP_011537058.1:p.Lys2185Gln
XM_011538757.3:c.6553A>C	XP_011537059.1:p.Lys2185Gln
XM_011538758.3:c.6553A>C	XP_011537060.1:p.Lys2185Gln
XM_011538759.2:c.6553A>C	XP_011537061.1:p.Lys2185Gln
XM_011538760.2:c.6553A>C	XP_011537062.1:p.Lys2185Gln
XM_011538761.2:c.6553A>C	XP_011537063.1:p.Lys2185Gln
XM_011538762.3:c.5785A>C	XP_011537064.1:p.Lys1929Gln
XM_011538763.3:c.5692A>C	XP_011537065.1:p.Lys1898Gln
XM_011538764.3:c.6553A>C	XP_011537066.1:p.Lys2185Gln
XM_011538765.3:c.6553A>C	XP_011537067.1:p.Lys2185Gln
XM_011538766.3:c.5014A>C	XP_011537068.1:p.Lys1672Gln
XM_017019980.2:c.6553A>C	XP_016875469.1:p.Lys2185Gln
XM_017019981.2:c.6553A>C	XP_016875470.1:p.Lys2185Gln
XM_017019982.1:c.6553A>C	XP_016875471.1:p.Lys2185Gln
XM_017019983.2:c.5671A>C	XP_016875472.1:p.Lys1891Gln
XR_001748869.1:n.6897A>C
XR_001748870.2:n.6897A>C
NM_025114.4:c.5692A>C MANE Select	NP_079390.3:p.Lys1898Gln