Human (GRCh38.p14)
Description

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

Location
About this transcript

This transcript has 8 exons, is annotated with 1 domain and feature, is associated with 2466 variant alleles and maps to 181 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 ENSP00000420069.1