Human (GRCh38.p14)
Description

translocase of inner mitochondrial membrane 23 homolog B [Source:HGNC Symbol;Acc:HGNC:23581]

Gene Synonyms

BA592B15.7

Location
About this transcript

This transcript has 7 exons, is annotated with 7 domains and features, is associated with 14731 variant alleles and maps to 486 oligo probes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000651259.3TIMM23B-2032495188aaENSP00000502369.1
 
Protein coding
CCDS73131Q5SRD1-1 NM_001290117.2MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1
ENST00000652716.1TIMM23B-2041152140aaENSP00000502146.1
 
Protein coding
CCDS76301Q5SRD1-2 -GENCODE basic
ENST00000478381.5TIMM23B-201262399aaENSP00000502398.1
 
Nonsense mediated decay
A0A6Q8PGT7 -TSL:2
ENST00000483296.5TIMM23B-2021156No protein-
 
Protein coding CDS not defined
--TSL:2
Statistics

Exons: 7, Coding exons: 7, Transcript length: 2,495 bps, Translation length: 188 residues

MANE

This MANE Select transcript contains ENSP00000502369 and matches to NM_001290117.2 and NP_001277046.1

Uniprot

This transcript corresponds to the following Uniprot identifiers: Q5SRD1

CCDS

This transcript is a member of the Human CCDS set: CCDS73131

Version

ENST00000651259.3

Type

Protein coding

Annotation Method

Manual annotation (determined on a case-by-case basis) from the Havana project.

GENCODE basic gene

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