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Human (GRCh38.p14)
Description

serpin family B member 12 [Source:HGNC Symbol;Acc:HGNC:14220]

Location
About this transcript

This transcript has 8 exons, is annotated with 12 domains and features, is associated with 11936 variant alleles and maps to 349 oligo probes.

Gene
Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000382768.2SERPINB12-2023738425aaENSP00000372218.1
 
Protein coding
CCDS77194Q96P63-2 NM_001307928.2MANE SelectEnsembl CanonicalGENCODE PrimaryGENCODE BasicAPPRIS P1TSL:1
ENST00000269491.6SERPINB12-2013678405aaENSP00000269491.1
 
Protein coding
CCDS11984Q96P63-1 -GENCODE PrimaryGENCODE BasicTSL:1
ENST00000680447.1SERPINB12-2031367No protein-
 
Protein coding CDS not defined
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Statistics

Exons: 8, Coding exons: 7, Transcript length: 3,678 bps, Translation length: 405 residues

Uniprot

This transcript corresponds to the following Uniprot identifiers: Q96P63

CCDS

This transcript is a member of the Human CCDS set: CCDS11984

Transcript Support Level (TSL)

TSL:1

Version

ENST00000269491.6

Type

Protein coding

Annotation Method

Manual annotation (determined on a case-by-case basis) from the Havana project.

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.