Human (GRCh38.p14)
Description

heterogeneous nuclear ribonucleoprotein R [Source:HGNC Symbol;Acc:HGNC:5047]

Gene Synonyms

HNRNP-R, HNRPR

Location

Scaffold HSCHR1_4_CTG3: 73,750-114,315 reverse strand.

GRCh38:KQ458383.1

View this gene on the primary assembly.

About this gene

This gene has 13 transcripts (splice variants), 1 gene allele and is associated with 2 phenotypes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000634713.1HNRNPR-2182691636aaENSP00000488945.1
 
Protein coding
O43390-2 -Ensembl CanonicalGENCODE basic
ENST00000634766.2HNRNPR-2197751633aaENSP00000489252.1
 
Protein coding
O43390-1 -GENCODE basic
ENST00000634634.2HNRNPR-2177683595aaENSP00000488941.1
 
Protein coding
O43390-3 -GENCODE basic
ENST00000635150.1HNRNPR-2237646535aaENSP00000489275.1
 
Protein coding
O43390-4 -GENCODE basic
ENST00000634808.2HNRNPR-2207574574aaENSP00000518723.1
 
Protein coding
--GENCODE basic
ENST00000634263.1HNRNPR-2142694633aaENSP00000489371.1
 
Protein coding
O43390-1 -GENCODE basic
ENST00000634427.4HNRNPR-2152518532aaENSP00000518725.1
 
Protein coding
--GENCODE basic
ENST00000634952.2HNRNPR-2222099481aaENSP00000518726.1
 
Protein coding
--GENCODE basic
ENST00000635199.1HNRNPR-2241837494aaENSP00000489386.1
 
Protein coding
B4DT28 -GENCODE basic
ENST00000641231.1HNRNPR-226646141aaENSP00000493186.1
 
Nonsense mediated decay
A0A286YEZ8 -CDS 5' incomplete
ENST00000635623.1HNRNPR-2251637No protein-
 
Protein coding CDS not defined
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ENST00000634492.1HNRNPR-216557No protein-
 
Protein coding CDS not defined
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ENST00000634921.1HNRNPR-221612No protein-
 
Retained intron
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