Canonical Allele Identifier: CA2815040515
Gene: PDYN HGNC NCBI
PDYN-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.1994021A>T , CM000682.2:g.1994021A>T GRCh38
NC_000020.10:g.1974667A>T , CM000682.1:g.1974667A>T GRCh37
NC_000020.9:g.1922667A>T NCBI36
NG_028027.1:g.5225T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000217305.3:c.-190T>A (PDYN) MANE Select ENSP00000217305.2:n.-190T>A
ENST00000650874.1:c.-130T>A (PDYN) ENSP00000498438.1:n.-130T>A
ENST00000651882.1:c.-187T>A (PDYN) ENSP00000498752.1:n.-187T>A
ENST00000217305.2:c.-190T>A (PDYN) ENSP00000217305.2:n.-190T>A
ENST00000539905.5:c.-130T>A (PDYN) ENSP00000440185.1:n.-130T>A
NM_001190898.2:c.-187T>A (PDYN) NP_001177827.1:n.-187T>A
NM_001190899.2:c.-130T>A (PDYN) NP_001177828.1:n.-130T>A
NM_024411.4:c.-190T>A (PDYN) NP_077722.1:n.-190T>A
XR_244229.1:n.1217-12911A>T (PDYN-AS1)
NR_134520.1:n.1253-12911A>T (PDYN-AS1)
NM_024411.5:c.-190T>A (PDYN) MANE Select NP_077722.1:n.-190T>A
NM_001190898.3:c.-187T>A (PDYN) NP_001177827.1:n.-187T>A