Canonical Allele Identifier: CA657400443
Gene: PDYN HGNC NCBI
PDYN-AS1 HGNC NCBI

Linked Data

COSMIC: COSN9122273
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.1994146T>A , CM000682.2:g.1994146T>A GRCh38
NC_000020.10:g.1974792T>A , CM000682.1:g.1974792T>A GRCh37
NC_000020.9:g.1922792T>A NCBI36
NG_028027.1:g.5100A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000651882.1:c.-312A>T (PDYN) ENSP00000498752.1:n.-312A>T
ENST00000539905.5:c.-255A>T (PDYN) ENSP00000440185.1:n.-255A>T
NM_001190898.2:c.-312A>T (PDYN) NP_001177827.1:n.-312A>T
NM_001190899.2:c.-255A>T (PDYN) NP_001177828.1:n.-255A>T
NM_024411.4:c.-315A>T (PDYN) NP_077722.1:n.-315A>T
XR_244229.1:n.1217-12786T>A (PDYN-AS1)
NR_134520.1:n.1253-12786T>A (PDYN-AS1)
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