Canonical Allele Identifier: CA2345900688
Gene: PDYN HGNC NCBI
PDYN-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.1994022G= , CM000682.2:g.1994022G= GRCh38
NC_000020.10:g.1974668G= , CM000682.1:g.1974668G= GRCh37
NC_000020.9:g.1922668G= NCBI36
NG_028027.1:g.5224C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000217305.3:c.-191C= (PDYN) MANE Select ENSP00000217305.2:n.-191C=
ENST00000650874.1:c.-131C= (PDYN) ENSP00000498438.1:n.-131C=
ENST00000651882.1:c.-188C= (PDYN) ENSP00000498752.1:n.-188C=
ENST00000217305.2:c.-191C= (PDYN) ENSP00000217305.2:n.-191C=
ENST00000539905.5:c.-131C= (PDYN) ENSP00000440185.1:n.-131C=
NM_001190898.2:c.-188C= (PDYN) NP_001177827.1:n.-188C=
NM_001190899.2:c.-131C= (PDYN) NP_001177828.1:n.-131C=
NM_024411.4:c.-191C= (PDYN) NP_077722.1:n.-191C=
XR_244229.1:n.1217-12910G= (PDYN-AS1)
NR_134520.1:n.1253-12910G= (PDYN-AS1)
NM_024411.5:c.-191C= (PDYN) MANE Select NP_077722.1:n.-191C=
NM_001190898.3:c.-188C= (PDYN) NP_001177827.1:n.-188C=