Human (GRCh38.p14)
Description

SMIM14 divergent transcript [Source:HGNC Symbol;Acc:HGNC:53455]

Location
About this transcript

This transcript has 6 exons, is associated with 11562 variant alleles and maps to 196 oligo probes.

Gene
Transcript IDNamebpProteinTranslation IDBiotypeCCDSRefSeq MatchFlags
ENST00000706646.1SMIM14-DT-2091121No protein-
 
lncRNA
-Ensembl CanonicalGENCODE basic
ENST00000529314.2SMIM14-DT-2023296No protein-
 
lncRNA
-GENCODE basicTSL:3
ENST00000526807.2SMIM14-DT-2013074No protein-
 
lncRNA
-TSL:5
ENST00000657228.1SMIM14-DT-2043036No protein-
 
lncRNA
--
ENST00000667934.1SMIM14-DT-2072615No protein-
 
lncRNA
--
ENST00000666863.1SMIM14-DT-2062585No protein-
 
lncRNA
--
ENST00000659162.1SMIM14-DT-2052155No protein-
 
lncRNA
--
ENST00000532680.1SMIM14-DT-203517No protein-
 
lncRNA
-TSL:5
ENST00000693190.1SMIM14-DT-208393No protein-
 
lncRNA
--
Statistics

Exons: 6, Coding exons: 0, Transcript length: 1,121 bps,

Version

ENST00000706646.1

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.