Human (GRCh38.p14)
Description

lamin B1 [Source:HGNC Symbol;Acc:HGNC:6637]

About this transcript

This transcript has 11 exons, is associated with 27441 variant alleles and maps to 517 oligo probes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000261366.10LMNB1-2012890586aaENSP00000261366.5
 
Protein coding
CCDS4140P20700 NM_005573.4MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENST00000395354.1LMNB1-2021572387aaENSP00000378761.1
 
Protein coding
E9PBF6 -GENCODE basicTSL:1
ENST00000492190.5LMNB1-206738166aaENSP00000486992.1
 
Protein coding
A0A0D9SFY5 -TSL:3CDS 3' incomplete
ENST00000460265.5LMNB1-2033475329aaENSP00000486528.1
 
Nonsense mediated decay
A0A0D9SFE5 -TSL:1
ENST00000504788.5LMNB1-2081801No protein-
 
Protein coding CDS not defined
--TSL:2
ENST00000472034.5LMNB1-205730No protein-
 
Protein coding CDS not defined
--TSL:3
ENST00000463908.2LMNB1-204557No protein-
 
Protein coding CDS not defined
--TSL:4
ENST00000494185.1LMNB1-207579No protein-
 
Retained intron
--TSL:2
Statistics

Exons: 11, Coding exons: 0, Transcript length: 1,801 bps,

Transcript Support Level (TSL)

TSL:2

Version

ENST00000504788.5

Type

Protein coding CDS not defined

Annotation Method

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