Human (GRCh38.p14)
Description

splicing factor SWAP [Source:HGNC Symbol;Acc:HGNC:10790]

Gene Synonyms

SFRS8, SWAP

Location

Chromosome 12: 131,711,081-131,799,738 forward strand.

GRCh38:CM000674.2

About this gene

This gene has 11 transcripts (splice variants), 209 orthologues and 1 paralogue.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000261674.9SFSWAP-2013246951aaENSP00000261674.4
 
Protein coding
CCDS9273Q12872-1 NM_004592.4MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P4TSL:1
ENST00000541286.5SFSWAP-21032191003aaENSP00000437738.1
 
Protein coding
CCDS58290Q12872-2 -GENCODE basicAPPRIS ALT1TSL:1
ENST00000537164.1SFSWAP-205961320aaENSP00000439957.1
 
Protein coding
H0YFR9 -TSL:5CDS 5' and 3' incomplete
ENST00000538548.5SFSWAP-2072636121aaENSP00000445832.1
 
Nonsense mediated decay
F5H1A5 -TSL:5
ENST00000539506.5SFSWAP-2083149No protein-
 
Protein coding CDS not defined
--TSL:5
ENST00000542813.2SFSWAP-211373No protein-
 
Protein coding CDS not defined
--TSL:3
ENST00000535236.5SFSWAP-2035593No protein-
 
Retained intron
--TSL:1
ENST00000540469.5SFSWAP-2093536No protein-
 
Retained intron
--TSL:3
ENST00000537582.1SFSWAP-2061576No protein-
 
Retained intron
--TSL:2
ENST00000535399.1SFSWAP-204778No protein-
 
Retained intron
--TSL:2
ENST00000535202.1SFSWAP-202567No protein-
 
Retained intron
--TSL:2