Canonical Allele Identifier: CA2345900738
Gene: PDYN HGNC NCBI
PDYN-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.1994117C= , CM000682.2:g.1994117C= GRCh38
NC_000020.10:g.1974763C= , CM000682.1:g.1974763C= GRCh37
NC_000020.9:g.1922763C= NCBI36
NG_028027.1:g.5129G=

Transcript Alleles

HGVS Amino-acid change
ENST00000651882.1:c.-283G= (PDYN) ENSP00000498752.1:n.-283G=
ENST00000539905.5:c.-226G= (PDYN) ENSP00000440185.1:n.-226G=
NM_001190898.2:c.-283G= (PDYN) NP_001177827.1:n.-283G=
NM_001190899.2:c.-226G= (PDYN) NP_001177828.1:n.-226G=
NM_024411.4:c.-286G= (PDYN) NP_077722.1:n.-286G=
XR_244229.1:n.1217-12815C= (PDYN-AS1)
NR_134520.1:n.1253-12815C= (PDYN-AS1)