Canonical Allele Identifier: CA2651618136
Gene: PDYN HGNC NCBI
PDYN-AS1 HGNC NCBI

Linked Data

gnomAD v4: 20-1994029-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.1994029C>T , CM000682.2:g.1994029C>T GRCh38
NC_000020.10:g.1974675C>T , CM000682.1:g.1974675C>T GRCh37
NC_000020.9:g.1922675C>T NCBI36
NG_028027.1:g.5217G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000217305.3:c.-198G>A (PDYN) MANE Select ENSP00000217305.2:n.-198G>A
ENST00000650874.1:c.-138G>A (PDYN) ENSP00000498438.1:n.-138G>A
ENST00000651882.1:c.-195G>A (PDYN) ENSP00000498752.1:n.-195G>A
ENST00000217305.2:c.-198G>A (PDYN) ENSP00000217305.2:n.-198G>A
ENST00000539905.5:c.-138G>A (PDYN) ENSP00000440185.1:n.-138G>A
NM_001190898.2:c.-195G>A (PDYN) NP_001177827.1:n.-195G>A
NM_001190899.2:c.-138G>A (PDYN) NP_001177828.1:n.-138G>A
NM_024411.4:c.-198G>A (PDYN) NP_077722.1:n.-198G>A
XR_244229.1:n.1217-12903C>T (PDYN-AS1)
NR_134520.1:n.1253-12903C>T (PDYN-AS1)
NM_024411.5:c.-198G>A (PDYN) MANE Select NP_077722.1:n.-198G>A
NM_001190898.3:c.-195G>A (PDYN) NP_001177827.1:n.-195G>A
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