Human (GRCh38.p14)
Description

minichromosome maintenance complex component 5 [Source:HGNC Symbol;Acc:HGNC:6948]

Gene Synonyms

CDC46

Location

Chromosome 22: 35,400,134-35,425,431 forward strand.

GRCh38:CM000684.2

About this gene

This gene has 10 transcripts (splice variants), 203 orthologues, 8 paralogues and is associated with 1 phenotype.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000216122.9MCM5-2013458734aaENSP00000216122.3
 
Protein coding
CCDS13915B1AHB0 P33992 NM_006739.4MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENST00000382011.9MCM5-2022402691aaENSP00000371441.5
 
Protein coding
B1AHB1 -GENCODE basicTSL:2
ENST00000416905.1MCM5-203739230aaENSP00000393977.1
 
Protein coding
B1AHA9 -TSL:3CDS 3' incomplete
ENST00000444778.1MCM5-205551150aaENSP00000408705.1
 
Protein coding
B1AHB2 -TSL:5CDS 3' incomplete
ENST00000451351.5MCM5-20645057aaENSP00000412847.1
 
Nonsense mediated decay
F8WFD7 -TSL:4
ENST00000465557.1MCM5-208587No protein-
 
Protein coding CDS not defined
--TSL:4
ENST00000417343.1MCM5-204557No protein-
 
Protein coding CDS not defined
--TSL:5
ENST00000464908.5MCM5-207554No protein-
 
Protein coding CDS not defined
--TSL:4
ENST00000493569.5MCM5-210468No protein-
 
Protein coding CDS not defined
--TSL:3
ENST00000493076.5MCM5-2094599No protein-
 
Retained intron
--TSL:2