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Human (GRCh38.p14)
Description

TBC1 domain family member 32 [Source:HGNC Symbol;Acc:HGNC:21485]

Gene Synonyms

BA57L9.1, BROMI, C6ORF170, C6ORF171, DJ310J6.1, FLJ30899, FLJ34235

Location

Chromosome 6: 121,079,494-121,334,745 reverse strand.

GRCh38:CM000668.2

About this gene

This gene has 9 transcripts (splice variants), 192 orthologues, 1 paralogue and is associated with 2 phenotypes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000398212.7TBC1D32-20451011257aaENSP00000381270.2
 
Protein coding
CCDS43501Q96NH3-1 NM_152730.6MANE SelectEnsembl CanonicalGENCODE PrimaryGENCODE BasicTSL:5
ENST00000275159.11TBC1D32-20152241298aaENSP00000275159.6
 
Protein coding
CCDS93996Q96NH3-4 -GENCODE PrimaryGENCODE BasicAPPRIS P1TSL:5
ENST00000422369.1TBC1D32-205770213aaENSP00000397993.1
 
Protein coding
A2A304 -TSL:3CDS 3' incomplete
ENST00000464622.5TBC1D32-2065323108aaENSP00000428839.1
 
Nonsense mediated decay
Q96NH3-5 -TSL:2
ENST00000509492.2TBC1D32-20775467aaENSP00000429928.1
 
Nonsense mediated decay
H0YBP0 -TSL:3CDS 5' incomplete
ENST00000398197.6TBC1D32-2032690No protein-
 
Protein coding CDS not defined
--TSL:2
ENST00000368464.7TBC1D32-202906No protein-
 
Protein coding CDS not defined
--TSL:3
ENST00000523345.1TBC1D32-209429No protein-
 
Protein coding CDS not defined
--TSL:5
ENST00000519972.1TBC1D32-208369No protein-
 
Retained intron
--TSL:3