Human (GRCh37.p13)
Description

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

Gene Synonyms

AVT2, FLJ39822

Location

Chromosome 2: 165,752,696-165,812,035 reverse strand.

GRCh37:CM000664.1

About this gene

This gene has 10 transcripts (splice variants) and 6 paralogues.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeqFlags
ENST00000303735.4SLC38A11-0013737384aaENSP00000306178.4
 
Protein coding
CCDS2224Q08AI6 NM_173512.2GENCODE basic
ENST00000409058.1SLC38A11-0021647437aaENSP00000387345.1
 
Protein coding
B8ZZ86 -GENCODE basic
ENST00000409149.3SLC38A11-0031621406aaENSP00000386272.3
 
Protein coding
CCDS56142Q08AI6 NM_001199148.1GENCODE basic
ENST00000409662.1SLC38A11-0091542406aaENSP00000386774.1
 
Protein coding
CCDS56142Q08AI6 -GENCODE basic
ENST00000424914.1SLC38A11-010452150aaENSP00000401448.1
 
Protein coding
H7C1P1 -CDS 5' and 3' incomplete
ENST00000493887.1SLC38A11-005577No protein-
 
Processed transcript
---
ENST00000483641.1SLC38A11-007786No protein-
 
Retained intron
---
ENST00000492134.1SLC38A11-004785No protein-
 
Retained intron
---
ENST00000470576.1SLC38A11-008696No protein-
 
Retained intron
---
ENST00000465898.1SLC38A11-006683No protein-
 
Retained intron
---