Human (GRCh38.p14)
Description

cytochrome P450 family 39 subfamily A member 1 [Source:HGNC Symbol;Acc:HGNC:17449]

Location
About this transcript

This transcript has 12 exons, is annotated with 29 domains and features, is associated with 42888 variant alleles and maps to 528 oligo probes.

Gene
Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000275016.3CYP39A1-2012432469aaENSP00000275016.2
 
Protein coding
CCDS4916Q9NYL5 NM_016593.5MANE SelectEnsembl CanonicalGENCODE PrimaryGENCODE BasicAPPRIS P1TSL:1
ENST00000889607.1CYP39A1-2062493437aaENSP00000559666.1
 
Protein coding
--GENCODE Basic
ENST00000889608.1CYP39A1-2072492523aaENSP00000559667.1
 
Protein coding
--GENCODE Basic
ENST00000619708.4CYP39A1-2052269297aaENSP00000477769.1
 
Protein coding
CCDS75465A0A087WTD2 -GENCODE PrimaryGENCODE BasicTSL:1
ENST00000889609.1CYP39A1-2082004401aaENSP00000559668.1
 
Protein coding
--GENCODE PrimaryGENCODE Basic
ENST00000889610.1CYP39A1-2091468248aaENSP00000559669.1
 
Protein coding
--GENCODE Basic
ENST00000489657.1CYP39A1-204506No protein-
 
Protein coding CDS not defined
--TSL:3
ENST00000480804.1CYP39A1-203403No protein-
 
Protein coding CDS not defined
--TSL:5
ENST00000476076.1CYP39A1-202277No protein-
 
Protein coding CDS not defined
--TSL:5
Statistics

Exons: 12, Coding exons: 12, Transcript length: 2,432 bps, Translation length: 469 residues

MANE

This MANE Select transcript contains ENSP00000275016 and matches to NM_016593.5 and NP_057677.2

Uniprot

This transcript corresponds to the following Uniprot identifiers: Q9NYL5

CCDS

This transcript is a member of the Human CCDS set: CCDS4916

Transcript Support Level (TSL)

TSL:1

Version

ENST00000275016.3

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.

GENCODE primary gene

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