Human (GRCh38.p14)
Description

serpin family B member 13 [Source:HGNC Symbol;Acc:HGNC:8944]

Gene Synonyms

HUR7, PI13

Location
About this transcript

This transcript has 8 exons, is annotated with 12 domains and features, is associated with 5762 variant alleles and maps to 517 oligo probes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000344731.10SERPINB13-2023130391aaENSP00000341584.6
 
Protein coding
CCDS11985Q9UIV8-1 NM_012397.4MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENST00000269489.9SERPINB13-2013206400aaENSP00000269489.6
 
Protein coding
CCDS77195A0A0A0MQW3 -GENCODE basicTSL:1
ENST00000415733.1SERPINB13-2031018124aaENSP00000391156.1
 
Protein coding
H7BZS9 -TSL:3CDS 5' incomplete
ENST00000431153.5SERPINB13-204580158aaENSP00000388300.1
 
Protein coding
C9JL93 -TSL:4CDS 3' incomplete
ENST00000438844.1SERPINB13-2052805165aaENSP00000394592.1
 
Nonsense mediated decay
F8WE70 -TSL:1
ENST00000479842.1SERPINB13-206600No protein-
 
Retained intron
--TSL:3
Statistics

Exons: 8, Coding exons: 7, Transcript length: 3,130 bps, Translation length: 391 residues

MANE

This MANE Select transcript contains ENSP00000341584 and matches to NM_012397.4 and NP_036529.1

Uniprot

This transcript corresponds to the following Uniprot identifiers: Q9UIV8

CCDS

This transcript is a member of the Human CCDS set: CCDS11985

Transcript Support Level (TSL)

TSL:1

Version

ENST00000344731.10

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.