Human (GRCh38.p14)
Description

Sp1 transcription factor [Source:HGNC Symbol;Acc:HGNC:11205]

Location
About this transcript

This transcript has 6 exons, is annotated with 35 domains and features, is associated with 18895 variant alleles and maps to 652 oligo probes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000327443.9SP1-2017680785aaENSP00000329357.4
 
Protein coding
CCDS8857P08047-1 NM_138473.3MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P4TSL:1
ENST00000426431.2SP1-2027603778aaENSP00000404263.2
 
Protein coding
CCDS44898P08047-2 -GENCODE basicAPPRIS ALT1TSL:1
ENST00000548560.1SP1-2031061230aaENSP00000458133.1
 
Protein coding
H3BVI2 -TSL:2CDS 3' incomplete
ENST00000551969.5SP1-204602162aaENSP00000457804.1
 
Protein coding
H3BUU5 -TSL:3CDS 3' incomplete
Statistics

Exons: 6, Coding exons: 5, Transcript length: 7,603 bps, Translation length: 778 residues

Uniprot

This transcript corresponds to the following Uniprot identifiers: P08047

CCDS

This transcript is a member of the Human CCDS set: CCDS44898

Transcript Support Level (TSL)

TSL:1

Version

ENST00000426431.2

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.