Human (GRCh38.p14)
Description

laminin subunit alpha 5 [Source:HGNC Symbol;Acc:HGNC:6485]

Location
About this transcript

This transcript has 80 exons, is annotated with 201 domains and features, is associated with 40024 variant alleles and maps to 2034 oligo probes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000252999.7LAMA5-201114263695aaENSP00000252999.3
 
Protein coding
CCDS33502O15230-1 NM_005560.6MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENST00000497053.2LAMA5-213723241aaENSP00000481814.1
 
Protein coding
A0A087WYH7 -TSL:3CDS 5' and 3' incomplete
ENST00000474128.1LAMA5-20857938aaENSP00000420069.1
 
Nonsense mediated decay
H7C5J6 -TSL:3CDS 5' incomplete
ENST00000370677.4LAMA5-2021674No protein-
 
Protein coding CDS not defined
--TSL:2
ENST00000492698.1LAMA5-211894No protein-
 
Protein coding CDS not defined
--TSL:3
ENST00000497363.1LAMA5-214579No protein-
 
Protein coding CDS not defined
--TSL:3
ENST00000370691.6LAMA5-2033160No protein-
 
Retained intron
--TSL:1
ENST00000495695.1LAMA5-212780No protein-
 
Retained intron
--TSL:2
ENST00000491036.2LAMA5-210728No protein-
 
Retained intron
--TSL:2
ENST00000464134.1LAMA5-205637No protein-
 
Retained intron
--TSL:2
ENST00000462415.2LAMA5-204585No protein-
 
Retained intron
--TSL:2
ENST00000471042.1LAMA5-207487No protein-
 
Retained intron
--TSL:2
ENST00000481120.1LAMA5-209386No protein-
 
Retained intron
--TSL:2
ENST00000468786.1LAMA5-206325No protein-
 
Retained intron
--TSL:2

Protein domains for ENSP00000252999.3