Canonical Allele Identifier: CA385993010

Gene: CEP290

Linked Data

• MyVariant Identifiers: chr12:g.88476973G>C (hg19) ; chr12:g.88083196G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.88083196G>C , CM000674.2:g.88083196G>C	GRCh38
NC_000012.11:g.88476973G>C , CM000674.1:g.88476973G>C	GRCh37
NC_000012.10:g.87001104G>C	NCBI36
NG_008417.1:g.64021C>G
NG_008417.2:g.64021C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000309041.12:c.4847C>G	ENSP00000308021.8:p.Thr1616Ser
ENST00000547691.8:c.2131C>G
ENST00000552810.6:c.4847C>G MANE Select	ENSP00000448012.1:p.Thr1616Ser
ENST00000672414.2:c.*3018C>G	ENSP00000500729.1:n.*3018C>G
ENST00000672647.1:n.3207C>G
ENST00000673058.2:c.4847C>G	ENSP00000500665.2:p.Thr1616Ser
ENST00000674971.1:c.4847C>G	ENSP00000502194.1:p.Thr1616Ser
ENST00000675230.1:c.4826C>G	ENSP00000502503.1:p.Thr1609Ser
ENST00000675408.1:c.4847C>G	ENSP00000502298.1:p.Thr1616Ser
ENST00000675476.1:c.5708C>G	ENSP00000502161.1:p.Thr1903Ser
ENST00000675628.1:n.5074C>G
ENST00000675794.1:c.*3018C>G	ENSP00000502841.1:n.*3018C>G
ENST00000675833.1:c.5615C>G	ENSP00000502559.1:p.Thr1872Ser
ENST00000675894.1:n.1152C>G
ENST00000676074.1:c.4847C>G	ENSP00000502079.1:p.Thr1616Ser
ENST00000676181.1:n.3775C>G
ENST00000676363.1:n.10573C>G
ENST00000676448.1:c.*2760C>G	ENSP00000501987.1:n.*2760C>G
ENST00000309041.11:c.4853C>G	ENSP00000308021.7:p.Thr1618Ser
ENST00000547691.6:c.2027C>G	ENSP00000446905.1:p.Thr676Ser
ENST00000552810.5:c.4847C>G	ENSP00000448012.1:p.Thr1616Ser
NM_025114.3:c.4847C>G	NP_079390.3:p.Thr1616Ser
XM_011538756.1:c.5708C>G	XP_011537058.1:p.Thr1903Ser
XM_011538757.1:c.5708C>G	XP_011537059.1:p.Thr1903Ser
XM_011538758.1:c.5708C>G	XP_011537060.1:p.Thr1903Ser
XM_011538759.1:c.5708C>G	XP_011537061.1:p.Thr1903Ser
XM_011538760.1:c.5708C>G	XP_011537062.1:p.Thr1903Ser
XM_011538761.1:c.5708C>G	XP_011537063.1:p.Thr1903Ser
XM_011538762.1:c.4940C>G	XP_011537064.1:p.Thr1647Ser
XM_011538763.1:c.4847C>G	XP_011537065.1:p.Thr1616Ser
XM_011538764.1:c.5708C>G	XP_011537066.1:p.Thr1903Ser
XM_011538765.1:c.5708C>G	XP_011537067.1:p.Thr1903Ser
XM_011538766.1:c.4169C>G	XP_011537068.1:p.Thr1390Ser
XM_011538756.3:c.5708C>G	XP_011537058.1:p.Thr1903Ser
XM_011538757.3:c.5708C>G	XP_011537059.1:p.Thr1903Ser
XM_011538758.3:c.5708C>G	XP_011537060.1:p.Thr1903Ser
XM_011538759.2:c.5708C>G	XP_011537061.1:p.Thr1903Ser
XM_011538760.2:c.5708C>G	XP_011537062.1:p.Thr1903Ser
XM_011538761.2:c.5708C>G	XP_011537063.1:p.Thr1903Ser
XM_011538762.3:c.4940C>G	XP_011537064.1:p.Thr1647Ser
XM_011538763.3:c.4847C>G	XP_011537065.1:p.Thr1616Ser
XM_011538764.3:c.5708C>G	XP_011537066.1:p.Thr1903Ser
XM_011538765.3:c.5708C>G	XP_011537067.1:p.Thr1903Ser
XM_011538766.3:c.4169C>G	XP_011537068.1:p.Thr1390Ser
XM_017019980.2:c.5708C>G	XP_016875469.1:p.Thr1903Ser
XM_017019981.2:c.5708C>G	XP_016875470.1:p.Thr1903Ser
XM_017019982.1:c.5708C>G	XP_016875471.1:p.Thr1903Ser
XM_017019983.2:c.4826C>G	XP_016875472.1:p.Thr1609Ser
XR_001748869.1:n.6052C>G
XR_001748870.2:n.6052C>G
NM_025114.4:c.4847C>G MANE Select	NP_079390.3:p.Thr1616Ser