Human (GRCh38.p14)
Description

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

Location
About this transcript

This transcript has 11 exons, is associated with 2205 variant alleles and maps to 1284 oligo probes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSRefSeq MatchFlags
ENST00000568997.5SLX1A-SULT1A3-2052834No protein-
 
Retained intron
-TSL:2
ENST00000569959.5SLX1A-SULT1A3-2062424No protein-
 
Retained intron
-TSL:2
ENST00000566712.2SLX1A-SULT1A3-2032380No protein-
 
Retained intron
-TSL:2
ENST00000567520.5SLX1A-SULT1A3-2042227No protein-
 
Retained intron
-TSL:2
ENST00000561824.5SLX1A-SULT1A3-2011838No protein-
 
Retained intron
-TSL:2
ENST00000565342.5SLX1A-SULT1A3-2022195No protein-
 
lncRNA
-Ensembl CanonicalGENCODE PrimaryGENCODE BasicTSL:2
Statistics

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

Transcript Support Level (TSL)

TSL:2

Version

ENST00000565342.5

Type

LncRNA

Annotation Method

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

GENCODE basic gene

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

GENCODE primary gene

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