Human (GRCh38.p14)
Description

complement C9 [Source:HGNC Symbol;Acc:HGNC:1358]

Location

Chromosome 5: 39,284,140-39,371,324 reverse strand.

GRCh38:CM000667.2

About this gene

This gene has 7 transcripts (splice variants), 189 orthologues, 39 paralogues and is associated with 4 phenotypes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000263408.5C9-2012770559aaENSP00000263408.4
 
Protein coding
CCDS3929P02748 NM_001737.5MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P2TSL:1
ENST00000509186.6C9-2032744535aaENSP00000512235.1
 
Protein coding
A0A8Q3SI95 -GENCODE basicAPPRIS ALT2TSL:3
ENST00000695880.1C9-2042553516aaENSP00000512236.1
 
Protein coding
A0A8Q3SI37 -GENCODE basic
ENST00000695881.1C9-2052726473aaENSP00000512237.1
 
Nonsense mediated decay
A0A8Q3SI39 --
ENST00000695882.1C9-206922No protein-
 
Protein coding CDS not defined
---
ENST00000695883.1C9-2071459No protein-
 
Retained intron
---
ENST00000467285.1C9-202572No protein-
 
Retained intron
--TSL:2