Human (GRCh38.p14)
Description

complement C6 [Source:HGNC Symbol;Acc:HGNC:1339]

Location

Chromosome 5: 41,142,116-41,261,438 reverse strand.

GRCh38:CM000667.2

About this gene

This gene has 11 transcripts (splice variants), 205 orthologues, 39 paralogues and is associated with 2 phenotypes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000337836.10C6-2023691934aaENSP00000338861.5
 
Protein coding
CCDS3936P13671 NM_000065.5MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENST00000263413.7C6-2013661934aaENSP00000263413.3
 
Protein coding
CCDS3936P13671 -GENCODE basicAPPRIS P1TSL:1
ENST00000433294.2C6-2041238243aaENSP00000401578.2
 
Protein coding
C9JX36 -TSL:5
ENST00000417809.1C6-203530133aaENSP00000396565.1
 
Protein coding
C9JC72 -TSL:4CDS 3' incomplete
ENST00000475349.5C6-2071015No protein-
 
Protein coding CDS not defined
--TSL:3
ENST00000461473.1C6-205613No protein-
 
Protein coding CDS not defined
--TSL:3
ENST00000473450.1C6-206527No protein-
 
Protein coding CDS not defined
--TSL:4
ENST00000706655.1C6-2102297No protein-
 
Retained intron
---
ENST00000706654.1C6-2091358No protein-
 
Retained intron
---
ENST00000706656.1C6-2111168No protein-
 
Retained intron
---
ENST00000695764.1C6-208815No protein-
 
Retained intron
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