Canonical Allele Identifier: CA1014745090
Gene: PDYN HGNC NCBI
PDYN-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1988565056
gnomAD v3: 20-1994118-T-A
gnomAD v4: 20-1994118-T-A

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.1994118T>A , CM000682.2:g.1994118T>A GRCh38
NC_000020.10:g.1974764T>A , CM000682.1:g.1974764T>A GRCh37
NC_000020.9:g.1922764T>A NCBI36
NG_028027.1:g.5128A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000651882.1:c.-284A>T (PDYN) ENSP00000498752.1:n.-284A>T
ENST00000539905.5:c.-227A>T (PDYN) ENSP00000440185.1:n.-227A>T
NM_001190898.2:c.-284A>T (PDYN) NP_001177827.1:n.-284A>T
NM_001190899.2:c.-227A>T (PDYN) NP_001177828.1:n.-227A>T
NM_024411.4:c.-287A>T (PDYN) NP_077722.1:n.-287A>T
XR_244229.1:n.1217-12814T>A (PDYN-AS1)
NR_134520.1:n.1253-12814T>A (PDYN-AS1)