Human (GRCh38.p14)
Description

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

About this transcript

This transcript has 11 exons, is annotated with 45 domains and features, is associated with 27682 variant alleles and maps to 589 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

Protein domains for ENSP00000261366.5