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Human (GRCh38.p14)
Description

ribosomal protein S17 [Source:HGNC Symbol;Acc:HGNC:10397]

Gene Synonyms

ES17, MGC72007, RPS17L, RPS17L1, RPS17L2, S17

Location

Scaffold HSCHR15_5_CTG8: 325,859-329,670 reverse strand.

GRCh38:KI270850.1

View this gene on the primary assembly.

About this gene

This gene has 9 transcripts (splice variants), 1 gene allele and is associated with 1 phenotype.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000632419.1RPS17-2181909136aaENSP00000488464.1
 
Protein coding
H0YN88 -Ensembl CanonicalGENCODE PrimaryGENCODE BasicTSL:2
ENST00000617731.2RPS17-216592135aaENSP00000483755.1
 
Protein coding
P08708 -GENCODE BasicTSL:1
ENST00000632799.1RPS17-22152259aaENSP00000487741.1
 
Nonsense mediated decay
H0YN73 -TSL:3CDS 5' incomplete
ENST00000634150.1RPS17-2241922No protein-
 
Retained intron
--TSL:2
ENST00000632240.1RPS17-2171877No protein-
 
Retained intron
--TSL:2
ENST00000632592.1RPS17-220932No protein-
 
Retained intron
--TSL:5
ENST00000633731.1RPS17-222776No protein-
 
Retained intron
--TSL:1
ENST00000632530.1RPS17-219760No protein-
 
Retained intron
--TSL:2
ENST00000633919.1RPS17-223580No protein-
 
Retained intron
--TSL:2