Human (GRCh38.p14)
Description

CD93 molecule [Source:HGNC Symbol;Acc:HGNC:15855]

Gene Synonyms

C1QR(P), C1QR1, C1QRP, CDW93, DJ737E23.1, ECSM3, MXRA4

Location
About this transcript

This transcript has 2 exons, is annotated with 69 domains and features, is associated with 4288 variant alleles and maps to 499 oligo probes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000246006.5CD93-2016681652aaENSP00000246006.4
 
Protein coding
CCDS13149Q9NPY3 NM_012072.4MANE SelectEnsembl CanonicalGENCODE PrimaryGENCODE BasicAPPRIS P1TSL:1
ENST00000850633.1CD93-2033008652aaENSP00000520912.1
 
Nonsense mediated decay
CCDS13149---
ENST00000850635.1CD93-2052549652aaENSP00000520914.1
 
Nonsense mediated decay
CCDS13149---
ENST00000850634.1CD93-2042472652aaENSP00000520913.1
 
Nonsense mediated decay
CCDS13149---
ENST00000799105.1CD93-202489No protein-
 
Retained intron
---
Statistics

Exons: 2, Coding exons: 2, Transcript length: 6,681 bps, Translation length: 652 residues

MANE

This MANE Select transcript contains ENSP00000246006 and matches to NM_012072.4 and NP_036204.2

Uniprot

This transcript corresponds to the following Uniprot identifiers: Q9NPY3

CCDS

This transcript is a member of the Human CCDS set: CCDS13149

Transcript Support Level (TSL)

TSL:1

Version

ENST00000246006.5

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.

GENCODE primary gene

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