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Human (GRCh38.p14)
Description

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

Location

Chromosome 5: 39,283,982-39,371,324 reverse strand.

GRCh38:CM000667.2

About this gene

This gene has 16 transcripts (splice variants), 189 orthologues, 39 paralogues and is associated with 3 phenotypes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000263408.5C9-2012770559aaENSP00000263408.4
 
Protein coding
CCDS3929P02748 NM_001737.5MANE SelectEnsembl CanonicalGENCODE PrimaryGENCODE BasicAPPRIS P2TSL:1
ENST00000884641.1C9-2102905587aaENSP00000554700.1
 
Protein coding
--GENCODE PrimaryGENCODE Basic
ENST00000884640.1C9-2092793484aaENSP00000554699.1
 
Protein coding
--GENCODE PrimaryGENCODE Basic
ENST00000884642.1C9-2112758556aaENSP00000554701.1
 
Protein coding
--GENCODE BasicAPPRIS ALT2
ENST00000509186.6C9-2032744535aaENSP00000512235.1
 
Protein coding
A0A8Q3SI95 -GENCODE BasicAPPRIS ALT2TSL:3
ENST00000884639.1C9-2082673559aaENSP00000554698.1
 
Protein coding
CCDS3929--GENCODE PrimaryGENCODE BasicAPPRIS P2
ENST00000695880.1C9-2042553516aaENSP00000512236.1
 
Protein coding
A0A8Q3SI37 -GENCODE Basic
ENST00000884643.1C9-2122508474aaENSP00000554702.1
 
Protein coding
--GENCODE BasicAPPRIS ALT2
ENST00000884644.1C9-2131691442aaENSP00000554703.1
 
Protein coding
--GENCODE Basic
ENST00000884646.1C9-2151625426aaENSP00000554705.1
 
Protein coding
--GENCODE Basic
ENST00000884647.1C9-2161184292aaENSP00000554706.1
 
Protein coding
--GENCODE Basic
ENST00000884645.1C9-2141128260aaENSP00000554704.1
 
Protein coding
--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