Canonical Allele Identifier: CA2651618137
Gene: PDYN HGNC NCBI
PDYN-AS1 HGNC NCBI

Linked Data

gnomAD v4: 20-1994031-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.1994031G>A , CM000682.2:g.1994031G>A GRCh38
NC_000020.10:g.1974677G>A , CM000682.1:g.1974677G>A GRCh37
NC_000020.9:g.1922677G>A NCBI36
NG_028027.1:g.5215C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000217305.3:c.-200C>T (PDYN) MANE Select ENSP00000217305.2:n.-200C>T
ENST00000650874.1:c.-140C>T (PDYN) ENSP00000498438.1:n.-140C>T
ENST00000651882.1:c.-197C>T (PDYN) ENSP00000498752.1:n.-197C>T
ENST00000217305.2:c.-200C>T (PDYN) ENSP00000217305.2:n.-200C>T
ENST00000539905.5:c.-140C>T (PDYN) ENSP00000440185.1:n.-140C>T
NM_001190898.2:c.-197C>T (PDYN) NP_001177827.1:n.-197C>T
NM_001190899.2:c.-140C>T (PDYN) NP_001177828.1:n.-140C>T
NM_024411.4:c.-200C>T (PDYN) NP_077722.1:n.-200C>T
XR_244229.1:n.1217-12901G>A (PDYN-AS1)
NR_134520.1:n.1253-12901G>A (PDYN-AS1)
NM_024411.5:c.-200C>T (PDYN) MANE Select NP_077722.1:n.-200C>T
NM_001190898.3:c.-197C>T (PDYN) NP_001177827.1:n.-197C>T