Human (GRCh37.p13)
Description

complement component 5 [Source:HGNC Symbol;Acc:1331]

Gene Synonyms

C5a, C5b, CPAMD4

Location

Chromosome 9: 123,714,616-123,812,554 reverse strand.

GRCh37:CM000671.1

About this gene

This gene has 5 transcripts (splice variants), 8 paralogues and is associated with 2 phenotypes.

Show/hide columns (1 hidden)
  • Transcript ID
  • Name
  • bp
  • Protein
  • Translation ID
  • Biotype
  • CCDS
  • UniProt Match
  • RefSeq
  • Flags
Transcript IDNamebpProteinBiotypeCCDSUniProt MatchRefSeqFlags
ENST00000223642.1C5-00154621676aa
 
Protein coding
CCDS6826P01031 NM_001735.2Ensembl CanonicalGENCODE Basic
ENST00000466280.1C5-004540No protein
 
Processed transcript
---
ENST00000460578.1C5-005521No protein
 
Processed transcript
---
ENST00000489802.1C5-003382No protein
 
Processed transcript
---
ENST00000480188.1C5-002619No protein
 
Retained intron
---
Name

C5 (HGNC Symbol)

UniProtKB

This gene has proteins that correspond to the following UniProtKB identifiers: P01031

CCDS

This gene is a member of the Human CCDS set: CCDS6826.1

LRG

LRG_28 provides a stable genomic reference framework for describing sequence variants for this gene

Ensembl version

ENSG00000106804.6

Other assemblies

This gene maps to 120,952,338-121,050,276 in GRCh38 coordinates.

Gene type

Protein coding

Annotation method

Annotation for this gene includes both automatic annotation from Ensembl and Havana manual curation, see article.

Alternative genes

This gene corresponds to the following database identifiers:

Havana gene:
OTTHUMG00000020579 (version 2)

Basic Gene Annotations from GENCODE 19

The GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).

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Basic Gene Annotations from GENCODE 19

The GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).

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Contigs

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