Human (GRCh38.p14)
Description

PWP1 homolog, endonuclein [Source:HGNC Symbol;Acc:HGNC:17015]

Gene Synonyms

IEF-SSP-9502

Location

Chromosome 12: 107,685,766-107,713,462 forward strand.

GRCh38:CM000674.2

About this gene

This gene has 12 transcripts (splice variants) and 205 orthologues.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000412830.8PWP1-2012549501aaENSP00000387365.3
 
Protein coding
CCDS9114Q13610-1 NM_007062.3MANE SelectEnsembl CanonicalGENCODE PrimaryGENCODE BasicAPPRIS P3TSL:1
ENST00000920793.1PWP1-2072873498aaENSP00000590852.1
 
Protein coding
--GENCODE PrimaryGENCODE BasicAPPRIS ALT1
ENST00000920794.1PWP1-2082618524aaENSP00000590853.1
 
Protein coding
--GENCODE Basic
ENST00000867450.1PWP1-2062462464aaENSP00000537509.1
 
Protein coding
--GENCODE Basic
ENST00000945394.1PWP1-2111856497aaENSP00000615453.1
 
Protein coding
--GENCODE PrimaryGENCODE BasicAPPRIS ALT1
ENST00000541166.1PWP1-2021722439aaENSP00000445249.1
 
Protein coding
CCDS81735B4DJV5 -GENCODE BasicTSL:2
ENST00000920796.1PWP1-2101701448aaENSP00000590855.1
 
Protein coding
--GENCODE Basic
ENST00000945395.1PWP1-2121660443aaENSP00000615454.1
 
Protein coding
--GENCODE Basic
ENST00000920795.1PWP1-2091530390aaENSP00000590854.1
 
Protein coding
--GENCODE Basic
ENST00000547995.5PWP1-20456998aaENSP00000447770.1
 
Protein coding
F8VZ56 -TSL:4CDS 3' incomplete
ENST00000552760.5PWP1-205851147aaENSP00000448227.1
 
Nonsense mediated decay
Q13610-2 -TSL:2
ENST00000547120.1PWP1-203543No protein-
 
Retained intron
--TSL:1