Human (GRCh37.p13)
Description

SLX1A-SULT1A3 readthrough (NMD candidate) [Source:HGNC Symbol;Acc:44437]

Location
About this transcript

This transcript has 11 exons, is associated with 2204 variant alleles and maps to 1288 oligo probes.

Gene
Transcript IDNamebpProteinTranslation IDBiotypeCCDSRefSeqFlags
ENST00000565342.1SLX1A-SULT1A3-0012195No protein-
 
Processed transcript
-GENCODE basic
ENST00000568997.1SLX1A-SULT1A3-0042834No protein-
 
Retained intron
--
ENST00000569959.1SLX1A-SULT1A3-0072424No protein-
 
Retained intron
--
ENST00000566712.1SLX1A-SULT1A3-0062380No protein-
 
Retained intron
--
ENST00000567520.1SLX1A-SULT1A3-0032227No protein-
 
Retained intron
--
ENST00000561824.1SLX1A-SULT1A3-0021838No protein-
 
Retained intron
--
Statistics

Exons: 11, Coding exons: 0, Transcript length: 2,195 bps,

Version

ENST00000565342.1

Type

Processed transcript

Annotation Method

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

Alternative transcripts

This transcript corresponds to the following database identifiers:

Havana transcript:
OTTHUMT00000434088 (version 1)
GENCODE basic gene

This transcript is a member of the Gencode basic gene set.