Human (GRCh37.p13)
Description

cullin 2 [Source:HGNC Symbol;Acc:2552]

Location
About this transcript

This transcript has 19 exons, is annotated with 18 domains and features, is associated with 27098 variant alleles and maps to 669 oligo probes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeqFlags
ENST00000374748.1CUL2-0024312745aaENSP00000363880.1
 
Protein coding
CCDS7179Q13617 Q5T2B4 -GENCODE basic
ENST00000374751.3CUL2-0014233745aaENSP00000363883.3
 
Protein coding
CCDS7179Q13617 Q5T2B4 NM_001198777.1GENCODE basic
ENST00000374749.3CUL2-0064208745aaENSP00000363881.3
 
Protein coding
CCDS7179Q13617 Q5T2B4 NM_003591.3GENCODE basic
ENST00000374746.1CUL2-0053903706aaENSP00000363878.1
 
Protein coding
Q5T2B4 Q5T2B5 -GENCODE basic
ENST00000602371.1CUL2-2032860688aaENSP00000473659.1
 
Protein coding
R4GNH8 -GENCODE basic
ENST00000374742.1CUL2-2012787706aaENSP00000363874.1
 
Protein coding
Q5T2B4 Q5T2B5 -GENCODE basic
ENST00000537177.1CUL2-2022376764aaENSP00000444856.1
 
Protein coding
CCDS55709Q13617 Q5T2B4 NM_001198779.1GENCODE basic
ENST00000421317.1CUL2-004767216aaENSP00000414095.1
 
Protein coding
Q5T2B4 -CDS 3' incomplete
ENST00000374754.4CUL2-007444090aaENSP00000363886.4
 
Nonsense mediated decay
Q5T2B7 --
ENST00000478044.1CUL2-003507No protein-
 
Processed transcript
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ENST00000468804.1CUL2-008479No protein-
 
Processed transcript
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