Human (GRCh38.p14)
Description

plasminogen [Source:HGNC Symbol;Acc:HGNC:9071]

Location

Chromosome 6: 160,702,194-160,754,097 forward strand.

GRCh38:CM000668.2

About this gene

This gene has 14 transcripts (splice variants), 235 orthologues, 14 paralogues and is associated with 4 phenotypes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000308192.14PLG-2023530810aaENSP00000308938.9
 
Protein coding
CCDS5279P00747 NM_000301.5MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENST00000418964.2PLG-2043580827aaENSP00000389424.2
 
Protein coding
A6PVI2 -GENCODE basicTSL:4
ENST00000297289.9PLG-2012416461aaENSP00000516619.1
 
Protein coding
--GENCODE basicTSL:5
ENST00000366924.6PLG-2031166136aaENSP00000355891.2
 
Protein coding
CCDS55074Q5TEH5 -GENCODE basicTSL:1
ENST00000494325.2PLG-212108361aaENSP00000516620.1
 
Protein coding
--GENCODE basicTSL:5
ENST00000706906.1PLG-2135213567aaENSP00000516618.1
 
Nonsense mediated decay
---
ENST00000462918.5PLG-206835No protein-
 
Protein coding CDS not defined
--TSL:2
ENST00000483038.5PLG-209757No protein-
 
Protein coding CDS not defined
--TSL:5
ENST00000461414.2PLG-205661No protein-
 
Protein coding CDS not defined
--TSL:5
ENST00000484367.5PLG-2102465No protein-
 
Retained intron
--TSL:1
ENST00000706907.1PLG-2141838No protein-
 
Retained intron
---
ENST00000471691.1PLG-208786No protein-
 
Retained intron
--TSL:2
ENST00000493435.1PLG-211582No protein-
 
Retained intron
--TSL:2
ENST00000467466.1PLG-207565No protein-
 
Retained intron
--TSL:2