Human (GRCh38.p14)
Description

FAM111A divergent transcript [Source:HGNC Symbol;Acc:HGNC:53752]

Location
About this transcript

This transcript has 5 exons, is associated with 5165 variant alleles and maps to 359 oligo probes.

Gene
Transcript IDNamebpProteinTranslation IDBiotypeCCDSRefSeq MatchFlags
ENST00000501817.6FAM111A-DT-2012110No protein-
 
lncRNA
-Ensembl CanonicalGENCODE basicTSL:5
ENST00000532845.2FAM111A-DT-2032659No protein-
 
lncRNA
-GENCODE basicTSL:3
ENST00000658798.1FAM111A-DT-2052063No protein-
 
lncRNA
--
ENST00000531708.1FAM111A-DT-202880No protein-
 
lncRNA
-TSL:5
ENST00000533220.1FAM111A-DT-204534No protein-
 
lncRNA
-TSL:2
Statistics

Exons: 5, Coding exons: 0, Transcript length: 2,110 bps,

Transcript Support Level (TSL)

TSL:5

Version

ENST00000501817.6

Type

LncRNA

Annotation Method

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

Annotation Attributes

dotter confirmed [Definitions]

GENCODE basic gene

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