The HNRNPA1 gene homepage

General information
Gene symbol HNRNPA1
Gene name heterogeneous nuclear ribonucleoprotein A1
Chromosome 12
Chromosomal band q13.1
Imprinted Unknown
Genomic reference NC_000012.11
Transcript reference NM_031157.2
Associated with diseases ALS-20, IBMPFD-3
Citation reference(s) -
Curators (1) Global Variome, with Curator vacancy
Total number of public variants reported 22
Unique public DNA variants reported 17
Individuals with public variants 4
Hidden variants 1
Date created September 13, 2012
Date last updated February 08, 2021
Version HNRNPA1:210208

Graphical displays and utilities
Graphs Graphs displaying summary information of all variants in the database »
UCSC Genome Browser Show variants in the UCSC Genome Browser (full view, compact view)
Ensembl Genome Browser Show variants in the Ensembl Genome Browser (full view, compact view)
NCBI Sequence Viewer Show distribution histogram of variants in the NCBI Sequence Viewer

Links to other resources
HGNC 5031
Entrez Gene 3178
PubMed articles HNRNPA1
OMIM - Gene 164017
OMIM - Diseases ALS-20 (sclerosis, lateral, amyotrophic, type 20 (ALS-20))
IBMPFD-3 (myopathy, inclusion body, with early-onset Paget disease with or without frontotemporal dementia, type 3 (IBMPFD-3))
GeneCards HNRNPA1
GeneTests HNRNPA1
Orphanet HNRNPA1

Active transcripts




NCBI ID     

NCBI Protein ID     

00001436 12 transcript variant 2 NM_031157.2 NP_112420.1 22

Copyright & disclaimer
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