Canonical Allele Identifier: CA2589570258
Gene: PDYN HGNC NCBI
PDYN-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs2122411293
gnomAD v3: 20-1994042-C-CA
gnomAD v4: 20-1994042-C-CA
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.1994045dup , CM000682.2:g.1994045dup GRCh38
NC_000020.10:g.1974691dup , CM000682.1:g.1974691dup GRCh37
NC_000020.9:g.1922691dup NCBI36
NG_028027.1:g.5203dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000217305.3:c.-212dup (PDYN) MANE Select ENSP00000217305.2:n.-212dup
ENST00000650874.1:c.-152dup (PDYN) ENSP00000498438.1:n.-152dup
ENST00000651882.1:c.-209dup (PDYN) ENSP00000498752.1:n.-209dup
ENST00000217305.2:c.-212dup (PDYN) ENSP00000217305.2:n.-212dup
ENST00000539905.5:c.-152dup (PDYN) ENSP00000440185.1:n.-152dup
NM_001190898.2:c.-209dup (PDYN) NP_001177827.1:n.-209dup
NM_001190899.2:c.-152dup (PDYN) NP_001177828.1:n.-152dup
NM_024411.4:c.-212dup (PDYN) NP_077722.1:n.-212dup
XR_244229.1:n.1217-12887dup (PDYN-AS1)
NR_134520.1:n.1253-12887dup (PDYN-AS1)
NM_024411.5:c.-212dup (PDYN) MANE Select NP_077722.1:n.-212dup
NM_001190898.3:c.-209dup (PDYN) NP_001177827.1:n.-209dup
Search 100 bp 5'
Search 100 bp 3'