Human (GRCh38.p14)
Description

ceruloplasmin [Source:HGNC Symbol;Acc:HGNC:2295]

Gene Synonyms

AB073614

Location

Chromosome 3: 149,162,410-149,221,829 reverse strand.

GRCh38:CM000665.2

About this gene

This gene has 15 transcripts (splice variants), 201 orthologues, 35 paralogues and is associated with 2 phenotypes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000264613.11CP-20144521065aaENSP00000264613.6
 
Protein coding
CCDS3141P00450 NM_000096.4MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENST00000494544.1CP-2132806852aaENSP00000420545.1
 
Protein coding
H7C5R1 -TSL:1CDS 5' incomplete
ENST00000479771.5CP-2091150225aaENSP00000420367.1
 
Protein coding
H7C5N5 -TSL:5CDS 5' incomplete
ENST00000455472.3CP-202571178aaENSP00000426888.1
 
Protein coding
D6RE86 -TSL:5CDS 3' incomplete
ENST00000481169.5CP-2103411946aaENSP00000418773.1
 
Nonsense mediated decay
E9PFZ2 -TSL:2
ENST00000462336.5CP-204607No protein-
 
Protein coding CDS not defined
--TSL:3
ENST00000490639.5CP-2123105No protein-
 
Retained intron
--TSL:1
ENST00000460674.5CP-2032269No protein-
 
Retained intron
--TSL:1
ENST00000489736.5CP-2111756No protein-
 
Retained intron
--TSL:1
ENST00000474204.1CP-208712No protein-
 
Retained intron
--TSL:2
ENST00000471356.1CP-206671No protein-
 
Retained intron
--TSL:2
ENST00000497797.5CP-214606No protein-
 
Retained intron
--TSL:2
ENST00000463556.5CP-205590No protein-
 
Retained intron
--TSL:2
ENST00000497902.5CP-215542No protein-
 
Retained intron
--TSL:2
ENST00000473296.1CP-207496No protein-
 
Retained intron
--TSL:3