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Human (GRCh38.p14)
Description

complement C8 gamma chain [Source:HGNC Symbol;Acc:HGNC:1354]

Location

Chromosome 9: 136,945,185-136,946,975 forward strand.

GRCh38:CM000671.2

About this gene

This gene has 6 transcripts (splice variants), 169 orthologues and is associated with 1 phenotype.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000371634.7C8G-201881202aaENSP00000360697.3
 
Protein coding
CCDS7017P07360 NM_000606.3MANE SelectEnsembl CanonicalGENCODE PrimaryGENCODE BasicAPPRIS P1TSL:3
ENST00000649480.1C8G-20548865aaENSP00000497839.1
 
Nonsense mediated decay
A0A3B3ITK5 -CDS 5' incomplete
ENST00000484376.1C8G-20343041aaENSP00000497973.1
 
Nonsense mediated decay
A0A3B3ITY0 -TSL:3CDS 5' incomplete
ENST00000647910.1C8G-204567No protein-
 
Protein coding CDS not defined
---
ENST00000649755.1C8G-206477No protein-
 
Retained intron
---
ENST00000465773.1C8G-202457No protein-
 
Retained intron
--TSL:3