Canonical Allele Identifier: CA385979442

Gene: CEP290

Linked Data

• MyVariant Identifiers: chr12:g.88456556C>G (hg19) ; chr12:g.88062779C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.88062779C>G , CM000674.2:g.88062779C>G	GRCh38
NC_000012.11:g.88456556C>G , CM000674.1:g.88456556C>G	GRCh37
NC_000012.10:g.86980687C>G	NCBI36
NG_008417.1:g.84438G>C
NG_008417.2:g.84438G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000309041.12:c.6280-1G>C	ENSP00000308021.8:n.6280-1G>C
ENST00000547691.8:c.3555-1G>C
ENST00000552810.6:c.6271-1G>C MANE Select	ENSP00000448012.1:n.6271-1G>C
ENST00000672414.2:c.*4442-1G>C	ENSP00000500729.1:n.*4442-1G>C
ENST00000672647.1:n.4631-1G>C
ENST00000673058.2:c.6271-1G>C	ENSP00000500665.2:n.6271-1G>C
ENST00000674889.1:n.3224-1G>C
ENST00000674971.1:c.6271-1G>C	ENSP00000502194.1:n.6271-1G>C
ENST00000675230.1:c.6250-1G>C	ENSP00000502503.1:n.6250-1G>C
ENST00000675408.1:c.6271-1G>C	ENSP00000502298.1:n.6271-1G>C
ENST00000675476.1:c.7132-1G>C	ENSP00000502161.1:n.7132-1G>C
ENST00000675628.1:n.6498-1G>C
ENST00000675794.1:c.*4442-1G>C	ENSP00000502841.1:n.*4442-1G>C
ENST00000675833.1:c.7039-1G>C	ENSP00000502559.1:n.7039-1G>C
ENST00000675894.1:n.2576-1G>C
ENST00000676074.1:c.6271-1G>C	ENSP00000502079.1:n.6271-1G>C
ENST00000676181.1:n.5199-1G>C
ENST00000676190.1:n.710-1G>C
ENST00000676363.1:n.11997-1G>C
ENST00000309041.11:c.6277-1G>C	ENSP00000308021.7:n.6277-1G>C
ENST00000547691.6:c.3451-1G>C	ENSP00000446905.1:n.3451-1G>C
ENST00000552810.5:c.6271-1G>C	ENSP00000448012.1:n.6271-1G>C
NM_025114.3:c.6271-1G>C	NP_079390.3:n.6271-1G>C
XM_011538756.1:c.7141-1G>C	XP_011537058.1:n.7141-1G>C
XM_011538757.1:c.7141-1G>C	XP_011537059.1:n.7141-1G>C
XM_011538758.1:c.7138-1G>C	XP_011537060.1:n.7138-1G>C
XM_011538759.1:c.7132-1G>C	XP_011537061.1:n.7132-1G>C
XM_011538760.1:c.7141-1G>C	XP_011537062.1:n.7141-1G>C
XM_011538761.1:c.7141-1G>C	XP_011537063.1:n.7141-1G>C
XM_011538762.1:c.6373-1G>C	XP_011537064.1:n.6373-1G>C
XM_011538763.1:c.6280-1G>C	XP_011537065.1:n.6280-1G>C
XM_011538766.1:c.5602-1G>C	XP_011537068.1:n.5602-1G>C
XR_945163.1:n.967+5759C>G
XM_011538756.3:c.7141-1G>C	XP_011537058.1:n.7141-1G>C
XM_011538757.3:c.7141-1G>C	XP_011537059.1:n.7141-1G>C
XM_011538758.3:c.7138-1G>C	XP_011537060.1:n.7138-1G>C
XM_011538759.2:c.7132-1G>C	XP_011537061.1:n.7132-1G>C
XM_011538760.2:c.7141-1G>C	XP_011537062.1:n.7141-1G>C
XM_011538761.2:c.7141-1G>C	XP_011537063.1:n.7141-1G>C
XM_011538762.3:c.6373-1G>C	XP_011537064.1:n.6373-1G>C
XM_011538763.3:c.6280-1G>C	XP_011537065.1:n.6280-1G>C
XM_011538766.3:c.5602-1G>C	XP_011537068.1:n.5602-1G>C
XM_017019980.2:c.7132-1G>C	XP_016875469.1:n.7132-1G>C
XM_017019981.2:c.7132-1G>C	XP_016875470.1:n.7132-1G>C
XM_017019982.1:c.7141-1G>C	XP_016875471.1:n.7141-1G>C
XM_017019983.2:c.6259-1G>C	XP_016875472.1:n.6259-1G>C
XR_001748869.1:n.7476-1G>C
XR_001748870.2:n.7476-1G>C
NM_025114.4:c.6271-1G>C MANE Select	NP_079390.3:n.6271-1G>C