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Human (GRCh37.p13)
Description

heterogeneous nuclear ribonucleoprotein A1 [Source:HGNC Symbol;Acc:5031]

Gene Synonyms

ALS19, ALS20, HNRPA1, HNRPA1L3, IBMPFD3, hnRNP A1, hnRNP-A1, hnRNPA1

Location

Chromosome 12: 54,673,977-54,680,872 forward strand.

GRCh37:CM000674.1

About this gene

This gene has 14 transcripts (splice variants), 7 paralogues and is associated with 2 phenotypes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeqFlags
ENST00000546500.1HNRNPA1-0014121320aaENSP00000448617.1
 
Protein coding
CCDS41793F8VYN5 H0YH80 P09651
Q3MI39 Q9BSM5
-GENCODE basic
ENST00000340913.6HNRNPA1-0021842372aaENSP00000341826.6
 
Protein coding
CCDS44909F8VYN5 P09651 NM_002136
NM_031157
NP_002127
NP_112420
GENCODE basic
ENST00000547276.1HNRNPA1-0121539267aaENSP00000447260.1
 
Protein coding
F8VYN5 P09651 -GENCODE basic
ENST00000330752.8HNRNPA1-0231294307aaENSP00000333504.8
 
Protein coding
F8VYN5 F8W6I7 -GENCODE basic
ENST00000550482.1HNRNPA1-018832191aaENSP00000446486.1
 
Protein coding
H0YH80 Q3MI39 -CDS 5' incomplete
ENST00000548688.1HNRNPA1-013711231aaENSP00000447782.1
 
Protein coding
F8VYN5 F8VZ49 -CDS 3' incomplete
ENST00000550994.1HNRNPA1-014569113aaENSP00000448917.1
 
Protein coding
F8VYN5 -CDS 3' incomplete
ENST00000547708.1HNRNPA1-015530156aaENSP00000448229.1
 
Protein coding
F8W646 -CDS 3' incomplete
ENST00000551702.1HNRNPA1-019481145aaENSP00000448117.1
 
Protein coding
F8VTQ5 -CDS 3' incomplete
ENST00000547566.1HNRNPA1-0061234320aaENSP00000449913.1
 
Nonsense mediated decay
CCDS41793F8VYN5 H0YH80 P09651
Q3MI39 Q9BSM5
--
ENST00000551803.1HNRNPA1-022372No protein-
 
Processed transcript
---
ENST00000551665.1HNRNPA1-021925No protein-
 
Retained intron
---
ENST00000547870.1HNRNPA1-016920No protein-
 
Retained intron
---
ENST00000551679.1HNRNPA1-020359No protein-
 
Retained intron
---

Gene-based displays