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Human (GRCh38.p14)
Description

serpin family B member 7 [Source:HGNC Symbol;Acc:HGNC:13902]

Location

Chromosome 18: 63,752,935-63,805,376 forward strand.

GRCh38:CM000680.2

About this gene

This gene has 7 transcripts (splice variants), 93 orthologues, 36 paralogues and is associated with 2 phenotypes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000398019.7SERPINB7-2022195380aaENSP00000381101.2
 
Protein coding
CCDS11988O75635-1 NM_003784.4MANE SelectEnsembl CanonicalGENCODE PrimaryGENCODE BasicAPPRIS P1TSL:1
ENST00000540675.5SERPINB7-2062193363aaENSP00000444572.1
 
Protein coding
CCDS58633O75635-2 -GENCODE BasicTSL:2
ENST00000336429.6SERPINB7-2011976380aaENSP00000337212.2
 
Protein coding
CCDS11988O75635-1 -GENCODE PrimaryGENCODE BasicAPPRIS P1TSL:1
ENST00000546027.5SERPINB7-2071951380aaENSP00000444861.1
 
Protein coding
CCDS11988O75635-1 -GENCODE BasicAPPRIS P1TSL:2
ENST00000425392.5SERPINB7-203587127aaENSP00000397301.1
 
Protein coding
C9JA68 -TSL:3CDS 3' incomplete
ENST00000447428.5SERPINB7-205561164aaENSP00000402362.1
 
Protein coding
C9JM00 -TSL:2CDS 3' incomplete
ENST00000431370.1SERPINB7-204560128aaENSP00000393947.1
 
Protein coding
A0A1B0GX82 -TSL:5CDS 3' incomplete