Human (GRCh38.p14)
Description

complement C9 [Source:HGNC Symbol;Acc:HGNC:1358]

Location
About this transcript

This transcript has 11 exons, is annotated with 122 domains and features, is associated with 36383 variant alleles and maps to 507 oligo probes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000263408.5C9-2012770559aaENSP00000263408.4
 
Protein coding
CCDS3929P02748 NM_001737.5MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P2TSL:1
ENST00000509186.6C9-2032744535aaENSP00000512235.1
 
Protein coding
A0A8Q3SI95 -GENCODE basicAPPRIS ALT2TSL:3
ENST00000695880.1C9-2042553516aaENSP00000512236.1
 
Protein coding
A0A8Q3SI37 -GENCODE basic
ENST00000695881.1C9-2052726473aaENSP00000512237.1
 
Nonsense mediated decay
A0A8Q3SI39 --
ENST00000695882.1C9-206922No protein-
 
Protein coding CDS not defined
---
ENST00000695883.1C9-2071459No protein-
 
Retained intron
---
ENST00000467285.1C9-202572No protein-
 
Retained intron
--TSL:2
Statistics

Exons: 11, Coding exons: 11, Transcript length: 2,770 bps, Translation length: 559 residues

MANE

This MANE Select transcript contains ENSP00000263408 and matches to NM_001737.5 and NP_001728.1

Uniprot

This transcript corresponds to the following Uniprot identifiers: P02748

CCDS

This transcript is a member of the Human CCDS set: CCDS3929

Transcript Support Level (TSL)

TSL:1

Version

ENST00000263408.5

Type

Protein coding

Annotation Method

Transcript where the Ensembl genebuild transcript and the Havana manual annotation have the same sequence, for every base pair. See article.

GENCODE basic gene

This transcript is a member of the Gencode basic gene set.