Human (GRCh38.p14)
Description

NME/NM23 family member 9 [Source:HGNC Symbol;Acc:HGNC:21343]

Gene Synonyms

NM23-H9, TXL-2, TXNDC6

About this transcript

This transcript has 11 exons, is annotated with 17 domains and features, is associated with 11386 variant alleles and maps to 378 oligo probes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000333911.9NME9-2022150330aaENSP00000335444.3
 
Protein coding
CCDS87142Q86XW9-1 NM_001349018.2MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENST00000383180.6NME9-2032133263aaENSP00000372667.2
 
Protein coding
CCDS3099Q86XW9-2 -GENCODE basicTSL:2
ENST00000317876.8NME9-2011930263aaENSP00000321929.4
 
Protein coding
CCDS3099Q86XW9-2 -GENCODE basicTSL:5
ENST00000484930.5NME9-207825261aaENSP00000419882.1
 
Protein coding
CCDS87141Q86XW9-3 -GENCODE basicTSL:5
ENST00000474690.5NME9-204800166aaENSP00000420435.1
 
Protein coding
H7C5P8 -TSL:3CDS 5' incomplete
ENST00000475751.5NME9-205660202aaENSP00000419147.1
 
Protein coding
C9JXP5 -TSL:3CDS 3' incomplete
ENST00000492993.5NME9-2091118174aaENSP00000419355.1
 
Nonsense mediated decay
Q3KNW3 -TSL:1
ENST00000488716.1NME9-20868889aaENSP00000420668.1
 
Nonsense mediated decay
F8WDB2 -TSL:3
ENST00000478220.5NME9-206579No protein-
 
Retained intron
--TSL:4

Protein domains for ENSP00000335444.3