Human (GRCh38.p14)
Description

FIGNL2 divergent transcript [Source:HGNC Symbol;Acc:HGNC:53299]

Location
About this transcript

This transcript has 3 exons, is associated with 2062 variant alleles and maps to 31 oligo probes.

Gene
Transcript IDNamebpProteinTranslation IDBiotypeCCDSRefSeq MatchFlags
ENST00000562996.1FIGNL2-DT-201427No protein-
 
lncRNA
-Ensembl CanonicalGENCODE PrimaryTSL:3
ENST00000782989.1FIGNL2-DT-2031342No protein-
 
lncRNA
-GENCODE Basic
ENST00000782992.1FIGNL2-DT-2061002No protein-
 
lncRNA
--
ENST00000782990.1FIGNL2-DT-204738No protein-
 
lncRNA
-GENCODE Basic
ENST00000782991.1FIGNL2-DT-205722No protein-
 
lncRNA
--
ENST00000782988.1FIGNL2-DT-202491No protein-
 
lncRNA
--
Statistics

Exons: 3, Coding exons: 0, Transcript length: 427 bps,

Transcript Support Level (TSL)

TSL:3

Version

ENST00000562996.1

Type

LncRNA

Annotation Method

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

GENCODE primary gene

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