Human (GRCh38.p14)
Description

cytochrome P450 family 4 subfamily A member 22 [Source:HGNC Symbol;Acc:HGNC:20575]

Location
About this transcript

This transcript has 12 exons, is annotated with 18 domains and features, is associated with 5876 variant alleles and maps to 756 oligo probes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000371891.8CYP4A22-2032535519aaENSP00000360958.3
 
Protein coding
CCDS30707Q5TCH4-1 NM_001010969.4MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENST00000619754.4CYP4A22-2062351357aaENSP00000482952.1
 
Protein coding
CCDS76160A0A087WZX9 -GENCODE basicTSL:1
ENST00000371890.7CYP4A22-2021780421aaENSP00000360957.3
 
Protein coding
Q5TCH5 -GENCODE basicTSL:5
ENST00000294337.7CYP4A22-2011725455aaENSP00000294337.3
 
Protein coding
A0A0C4DFN9 -GENCODE basicTSL:1
ENST00000485117.1CYP4A22-2041539No protein-
 
Protein coding CDS not defined
--TSL:5
ENST00000490948.5CYP4A22-2051523No protein-
 
Protein coding CDS not defined
--TSL:5
Statistics

Exons: 12, Coding exons: 12, Transcript length: 2,535 bps, Translation length: 519 residues

MANE

This MANE Select transcript contains ENSP00000360958 and matches to NM_001010969.4 and NP_001010969.2

Uniprot

This transcript corresponds to the following Uniprot identifiers: Q5TCH4

CCDS

This transcript is a member of the Human CCDS set: CCDS30707

Transcript Support Level (TSL)

TSL:1

Version

ENST00000371891.8

Type

Protein coding

Annotation Method

Transcript where the Ensembl genebuild transcript and the Havana manual annotation have the same sequence, for every base pair. See article.

GENCODE basic gene

This transcript is a member of the Gencode basic gene set.