Human (GRCh38.p14)
Description

solute carrier family 22 member 11 [Source:HGNC Symbol;Acc:HGNC:18120]

Gene Synonyms

OAT4

Location
About this transcript

This transcript has 3 exons, is associated with 1828 variant alleles and maps to 191 oligo probes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000301891.9SLC22A11-2013545550aaENSP00000301891.4
 
Protein coding
CCDS8074Q9NSA0-1 NM_018484.4MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENST00000377585.7SLC22A11-2032124442aaENSP00000366809.3
 
Protein coding
CCDS76425Q9NSA0-2 -GENCODE basicTSL:2
ENST00000377581.7SLC22A11-2021975481aaENSP00000366804.3
 
Protein coding
A6NCG2 -GENCODE basicTSL:5
ENST00000416590.1SLC22A11-204947153aaENSP00000413508.1
 
Protein coding
H7C3R9 -TSL:3CDS 5' incomplete
ENST00000428570.1SLC22A11-20597173aaENSP00000394043.1
 
Nonsense mediated decay
H7C0B7 -TSL:3CDS 5' incomplete
ENST00000490834.5SLC22A11-208894No protein-
 
Protein coding CDS not defined
--TSL:2
ENST00000478051.5SLC22A11-2071916No protein-
 
Retained intron
--TSL:5
ENST00000460745.1SLC22A11-2061845No protein-
 
Retained intron
--TSL:2
Statistics

Exons: 3, Coding exons: 2, Transcript length: 971 bps, Translation length: 73 residues

Transcript Support Level (TSL)

TSL:3

Incomplete CDS

CDS 5' incomplete

Version

ENST00000428570.1

Type

Nonsense mediated decay

Annotation Method

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