Human (GRCh38.p14)
Description

myelodysplastic syndrome 2 translocation associated [Source:HGNC Symbol;Acc:HGNC:29633]

Location
About this transcript

This transcript has 7 exons, is associated with 24946 variant alleles and maps to 308 oligo probes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSRefSeq MatchFlags
ENST00000477916.5MDS2-2021781No protein-
 
lncRNA
-Ensembl CanonicalGENCODE PrimaryGENCODE BasicTSL:1
ENST00000374555.7MDS2-2011029No protein-
 
lncRNA
-TSL:1
ENST00000795854.1MDS2-205831No protein-
 
lncRNA
--
ENST00000686180.2MDS2-203650No protein-
 
lncRNA
--
ENST00000686679.2MDS2-204602No protein-
 
lncRNA
--
ENST00000795855.1MDS2-206577No protein-
 
lncRNA
--
ENST00000795856.1MDS2-207489No protein-
 
lncRNA
--
Statistics

Exons: 7, Coding exons: 0, Transcript length: 1,781 bps,

Transcript Support Level (TSL)

TSL:1

Version

ENST00000477916.5

Type

LncRNA

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.

GENCODE primary gene

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