Human (GRCh38.p14)
Description

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

Location
About this transcript

This transcript has 15 exons, is associated with 60162 variant alleles and maps to 583 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: 15, Coding exons: 13, Transcript length: 1,876 bps, Translation length: 517 residues

Transcript Support Level (TSL)

TSL:2

Version

ENST00000479633.2

Type

Nonsense mediated decay

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.