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Human (GRCh38.p14)
Description

ARHGAP27P1-BPTFP1-KPNA2P3 readthrough, transcribed pseudogene [Source:HGNC Symbol;Acc:HGNC:52873]

Location
About this transcript

This transcript has 12 exons, is associated with 13365 variant alleles and maps to 793 oligo probes.

Gene
Transcript IDNamebpProteinTranslation IDBiotypeCCDSRefSeq MatchFlags
ENST00000578492.5ARHGAP27P1-BPTFP1-KPNA2P3-2012732No protein-
 
lncRNA
-Ensembl CanonicalGENCODE PrimaryTSL:2
ENST00000717267.1ARHGAP27P1-BPTFP1-KPNA2P3-2043760No protein-
 
lncRNA
-GENCODE Basic
ENST00000717266.1ARHGAP27P1-BPTFP1-KPNA2P3-2033289No protein-
 
lncRNA
-GENCODE Basic
ENST00000579125.1ARHGAP27P1-BPTFP1-KPNA2P3-2021318No protein-
 
lncRNA
-TSL:1
Statistics

Exons: 12, Coding exons: 0, Transcript length: 2,732 bps,

Transcript Support Level (TSL)

TSL:2

Version

ENST00000578492.5

Type

LncRNA

Annotation Method

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

Annotation Attributes

overlaps pseudogene [Definitions]

GENCODE primary gene

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