Canonical Allele Identifier: CA2345900749
Gene: PDYN HGNC NCBI
PDYN-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1988566104
gnomAD v4: 20-1994142-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.1994142C>T , CM000682.2:g.1994142C>T GRCh38
NC_000020.10:g.1974788C>T , CM000682.1:g.1974788C>T GRCh37
NC_000020.9:g.1922788C>T NCBI36
NG_028027.1:g.5104G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000651882.1:c.-308G>A (PDYN) ENSP00000498752.1:n.-308G>A
ENST00000539905.5:c.-251G>A (PDYN) ENSP00000440185.1:n.-251G>A
NM_001190898.2:c.-308G>A (PDYN) NP_001177827.1:n.-308G>A
NM_001190899.2:c.-251G>A (PDYN) NP_001177828.1:n.-251G>A
NM_024411.4:c.-311G>A (PDYN) NP_077722.1:n.-311G>A
XR_244229.1:n.1217-12790C>T (PDYN-AS1)
NR_134520.1:n.1253-12790C>T (PDYN-AS1)