Human (GRCh38.p14)
Description

ARHGAP19-SLIT1 readthrough (NMD candidate) [Source:HGNC Symbol;Acc:HGNC:48348]

Location
About this transcript

This transcript has 1 exon, is associated with 903 variant alleles and maps to 116 oligo probes.

Gene
Transcript IDNamebpProteinTranslation IDBiotypeCCDSRefSeq MatchFlags
ENST00000479633.2ARHGAP19-SLIT1-2021876517aaENSP00000473567.1
 
Nonsense mediated decay
-Ensembl CanonicalGENCODE basicAPPRIS P1TSL:2
ENST00000475285.2ARHGAP19-SLIT1-2012389No protein-
 
Retained intron
-TSL:NA
Statistics

Exons: 1, Coding exons: 0, Transcript length: 2,389 bps,

Transcript Support Level (TSL)

TSL:NA

Version

ENST00000475285.2

Type

Retained intron

Annotation Method

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