Human (GRCh38.p14)
Description

complement C7 [Source:HGNC Symbol;Acc:HGNC:1346]

Location

Chromosome 5: 40,909,492-41,020,216 forward strand.

GRCh38:CM000667.2

About this gene

This gene has 14 transcripts (splice variants), 247 orthologues, 39 paralogues and is associated with 2 phenotypes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000313164.10C7-2015716843aaENSP00000322061.9
 
Protein coding
CCDS47201P10643 NM_000587.4MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENST00000696333.1C7-2064011843aaENSP00000512566.1
 
Protein coding
CCDS47201P10643 -GENCODE basicAPPRIS P1
ENST00000696441.1C7-2082903800aaENSP00000512631.1
 
Protein coding
A0A8Q3SIM0 -GENCODE basic
ENST00000489457.2C7-204792164aaENSP00000512585.1
 
Protein coding
A0A8Q3WL76 -GENCODE basicTSL:3
ENST00000706664.1C7-2102922No protein-
 
Protein coding CDS not defined
---
ENST00000706666.1C7-2122495No protein-
 
Protein coding CDS not defined
---
ENST00000696442.1C7-209741No protein-
 
Protein coding CDS not defined
---
ENST00000494960.5C7-205714No protein-
 
Protein coding CDS not defined
--TSL:5
ENST00000706667.1C7-2134771No protein-
 
Retained intron
---
ENST00000706668.1C7-2144601No protein-
 
Retained intron
---
ENST00000706665.1C7-2111772No protein-
 
Retained intron
---
ENST00000486779.2C7-203843No protein-
 
Retained intron
--TSL:2
ENST00000464864.1C7-202738No protein-
 
Retained intron
--TSL:2
ENST00000696334.1C7-207403No protein-
 
Retained intron
---