Human (GRCh38.p14)
Description

SLX1B-SULT1A4 readthrough (NMD candidate) [Source:HGNC Symbol;Acc:HGNC:48353]

Location
About this transcript

This transcript has 9 exons, is associated with 1914 variant alleles and maps to 1088 oligo probes.

Gene
Transcript IDNamebpProteinTranslation IDBiotypeCCDSRefSeq MatchFlags
ENST00000564950.5SLX1B-SULT1A4-2032225No protein-
 
Retained intron
-Ensembl CanonicalTSL:2
ENST00000344620.10SLX1B-SULT1A4-2012424No protein-
 
Retained intron
-GENCODE basicTSL:2
ENST00000395400.4SLX1B-SULT1A4-2022380No protein-
 
Retained intron
-TSL:2
Statistics

Exons: 9, Coding exons: 0, Transcript length: 2,380 bps,

Transcript Support Level (TSL)

TSL:2

Version

ENST00000395400.4

Type

Retained intron

Annotation Method

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