Canonical Allele Identifier: CA310400400
Gene: PDYN HGNC NCBI
PDYN-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs946957133
gnomAD v3: 20-1994145-A-G
gnomAD v4: 20-1994145-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.1994145A>G , CM000682.2:g.1994145A>G GRCh38
NC_000020.10:g.1974791A>G , CM000682.1:g.1974791A>G GRCh37
NC_000020.9:g.1922791A>G NCBI36
NG_028027.1:g.5101T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000651882.1:c.-311T>C (PDYN) ENSP00000498752.1:n.-311T>C
ENST00000539905.5:c.-254T>C (PDYN) ENSP00000440185.1:n.-254T>C
NM_001190898.2:c.-311T>C (PDYN) NP_001177827.1:n.-311T>C
NM_001190899.2:c.-254T>C (PDYN) NP_001177828.1:n.-254T>C
NM_024411.4:c.-314T>C (PDYN) NP_077722.1:n.-314T>C
XR_244229.1:n.1217-12787A>G (PDYN-AS1)
NR_134520.1:n.1253-12787A>G (PDYN-AS1)