Human (GRCh38.p14)
Description

MISP family member 3 [Source:HGNC Symbol;Acc:HGNC:26963]

Location

Chromosome 19: 14,072,536-14,075,062 forward strand.

GRCh38:CM000681.2

View alleles of this gene on alternative sequences

About this gene

This gene has 4 transcripts (splice variants), 1 gene allele, 108 orthologues and 1 paralogue.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000587086.3MISP3-2021523219aaENSP00000465157.1
 
Protein coding
CCDS77246Q96FF7 NM_001291291.2MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENST00000269720.6MISP3-2011424361aaENSP00000269720.2
 
Protein coding
A0A044PY82 -GENCODE basicTSL:5
ENST00000590772.1MISP3-203708150aaENSP00000466176.1
 
Protein coding
K7ELQ6 -TSL:2CDS 5' incomplete
ENST00000591982.1MISP3-2042187No protein-
 
Retained intron
--TSL:NA