Human (GRCh38.p14)
Description

complement C5 [Source:HGNC Symbol;Acc:HGNC:1331]

Gene Synonyms

C5A, C5B, CPAMD4

Location

Chromosome 9: 120,932,987-121,075,195 reverse strand.

GRCh38:CM000671.2

About this gene

This gene has 13 transcripts (splice variants), 208 orthologues, 8 paralogues and is associated with 3 phenotypes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000223642.3C5-20154641676aaENSP00000223642.1
 
Protein coding
CCDS6826P01031 NM_001735.3MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENST00000696281.1C5-20869231682aaENSP00000512521.1
 
Protein coding
CCDS94473A0A8Q3SID6 -GENCODE basic
ENST00000466280.2C5-2031941567aaENSP00000513491.1
 
Protein coding
A0A8V8TMU5 -TSL:5CDS 5' incomplete
ENST00000697922.1C5-212694743aaENSP00000513478.1
 
Nonsense mediated decay
A0A8V8TN26 --
ENST00000696279.1C5-206686644aaENSP00000512520.1
 
Nonsense mediated decay
A0A8Q3SIH6 -CDS 5' incomplete
ENST00000696280.1C5-2076635No protein-
 
Protein coding CDS not defined
---
ENST00000696285.1C5-2102352No protein-
 
Protein coding CDS not defined
---
ENST00000460578.1C5-202521No protein-
 
Protein coding CDS not defined
--TSL:5
ENST00000489802.1C5-205382No protein-
 
Protein coding CDS not defined
--TSL:3
ENST00000697923.1C5-2139114No protein-
 
Retained intron
---
ENST00000480188.2C5-2046732No protein-
 
Retained intron
--TSL:2
ENST00000697921.1C5-2115424No protein-
 
Retained intron
---
ENST00000696284.1C5-2093321No protein-
 
Retained intron
---