Human (GRCh38.p14)
Description

cytochrome P450 family 4 subfamily F member 2 [Source:HGNC Symbol;Acc:HGNC:2645]

Location

Chromosome 19: 15,878,023-15,898,077 reverse strand.

GRCh38:CM000681.2

About this gene

This gene has 8 transcripts (splice variants), 441 orthologues and 12 paralogues.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000221700.11CYP4F2-2022361520aaENSP00000221700.3
 
Protein coding
CCDS12336P78329-1 NM_001082.5MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P3TSL:1
ENST00000011989.11CYP4F2-2012067520aaENSP00000011989.8
 
Protein coding
A0A0A0MQR0 -GENCODE basicAPPRIS ALT1TSL:1
ENST00000586927.2CYP4F2-204579153aaENSP00000465514.1
 
Protein coding
K7EK90 -TSL:4CDS 3' incomplete
ENST00000589654.2CYP4F2-20649974aaENSP00000467846.1
 
Protein coding
K7EQI8 -TSL:3CDS 5' incomplete
ENST00000587671.2CYP4F2-20595489aaENSP00000467443.2
 
Nonsense mediated decay
K7EPM0 -TSL:5
ENST00000392846.7CYP4F2-2032254No protein-
 
Retained intron
--TSL:2
ENST00000592710.1CYP4F2-207744No protein-
 
Retained intron
--TSL:3
ENST00000608168.1CYP4F2-208593No protein-
 
Retained intron
--TSL:3