Human (GRCh37.p13)
Description

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

Location
About this transcript

This transcript has 11 exons, is associated with 1968 variant alleles and maps to 1411 oligo probes.

Gene
Transcript IDNamebpProteinTranslation IDBiotypeCCDSRefSeqFlags
ENST00000564950.1SLX1B-SULT1A4-0012196No protein-
 
Sense overlapping
-GENCODE basic
Statistics

Exons: 11, Coding exons: 0, Transcript length: 2,196 bps,

Version

ENST00000564950.1

Type

Sense overlapping

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:
OTTHUMT00000433585 (version 1)
GENCODE basic gene

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