Human (GRCh38.p14)
Description

solute carrier family 38 member 11 [Source:HGNC Symbol;Acc:HGNC:26836]

Gene Synonyms

AVT2, FLJ39822

Location

Chromosome 2: 164,894,354-164,955,525 reverse strand.

GRCh38:CM000664.2

About this gene

This gene has 11 transcripts (splice variants), 201 orthologues and 15 paralogues.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000685975.1SLC38A11-2115750462aaENSP00000508649.1
 
Protein coding
CCDS92885A0A8I5QKK7 NM_001351537.2MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1
ENST00000303735.8SLC38A11-2013737384aaENSP00000306178.4
 
Protein coding
CCDS2224Q08AI6-2 -GENCODE basicTSL:2
ENST00000409058.5SLC38A11-2021647437aaENSP00000387345.1
 
Protein coding
B8ZZ86 -GENCODE basicTSL:5
ENST00000409149.7SLC38A11-2031621406aaENSP00000386272.3
 
Protein coding
CCDS56142Q08AI6-1 -GENCODE basicTSL:2
ENST00000409662.5SLC38A11-2041542406aaENSP00000386774.1
 
Protein coding
CCDS56142Q08AI6-1 -GENCODE basicTSL:1
ENST00000424914.1SLC38A11-205452150aaENSP00000401448.1
 
Protein coding
H7C1P1 -TSL:5CDS 5' and 3' incomplete
ENST00000493887.5SLC38A11-210577No protein-
 
Protein coding CDS not defined
--TSL:4
ENST00000483641.5SLC38A11-208786No protein-
 
Retained intron
--TSL:2
ENST00000492134.1SLC38A11-209785No protein-
 
Retained intron
--TSL:4
ENST00000470576.1SLC38A11-207696No protein-
 
Retained intron
--TSL:3
ENST00000465898.1SLC38A11-206683No protein-
 
Retained intron
--TSL:3