Canonical Allele Identifier: CA2345900692
Gene: PDYN HGNC NCBI
PDYN-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.1994041C= , CM000682.2:g.1994041C= GRCh38
NC_000020.10:g.1974687C= , CM000682.1:g.1974687C= GRCh37
NC_000020.9:g.1922687C= NCBI36
NG_028027.1:g.5205G=

Transcript Alleles

HGVS Amino-acid change
ENST00000217305.3:c.-210G= (PDYN) MANE Select ENSP00000217305.2:n.-210G=
ENST00000650874.1:c.-150G= (PDYN) ENSP00000498438.1:n.-150G=
ENST00000651882.1:c.-207G= (PDYN) ENSP00000498752.1:n.-207G=
ENST00000217305.2:c.-210G= (PDYN) ENSP00000217305.2:n.-210G=
ENST00000539905.5:c.-150G= (PDYN) ENSP00000440185.1:n.-150G=
NM_001190898.2:c.-207G= (PDYN) NP_001177827.1:n.-207G=
NM_001190899.2:c.-150G= (PDYN) NP_001177828.1:n.-150G=
NM_024411.4:c.-210G= (PDYN) NP_077722.1:n.-210G=
XR_244229.1:n.1217-12891C= (PDYN-AS1)
NR_134520.1:n.1253-12891C= (PDYN-AS1)
NM_024411.5:c.-210G= (PDYN) MANE Select NP_077722.1:n.-210G=
NM_001190898.3:c.-207G= (PDYN) NP_001177827.1:n.-207G=