Canonical Allele Identifier: CA310400283

Gene: PDYN PDYN-AS1

Linked Data

• dbSNP Id: rs534885878
• gnomAD v3: 20-1994045-A-T
• gnomAD v4: 20-1994045-A-T
• MyVariant Identifiers: chr20:g.1974691A>T (hg19) ; chr20:g.1994045A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.1994045A>T , CM000682.2:g.1994045A>T	GRCh38
NC_000020.10:g.1974691A>T , CM000682.1:g.1974691A>T	GRCh37
NC_000020.9:g.1922691A>T	NCBI36
NG_028027.1:g.5201T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000217305.3:c.-214T>A (PDYN) MANE Select	ENSP00000217305.2:n.-214T>A
ENST00000650874.1:c.-154T>A (PDYN)	ENSP00000498438.1:n.-154T>A
ENST00000651882.1:c.-211T>A (PDYN)	ENSP00000498752.1:n.-211T>A
ENST00000217305.2:c.-214T>A (PDYN)	ENSP00000217305.2:n.-214T>A
ENST00000539905.5:c.-154T>A (PDYN)	ENSP00000440185.1:n.-154T>A
NM_001190898.2:c.-211T>A (PDYN)	NP_001177827.1:n.-211T>A
NM_001190899.2:c.-154T>A (PDYN)	NP_001177828.1:n.-154T>A
NM_024411.4:c.-214T>A (PDYN)	NP_077722.1:n.-214T>A
XR_244229.1:n.1217-12887A>T (PDYN-AS1)
NR_134520.1:n.1253-12887A>T (PDYN-AS1)
NM_024411.5:c.-214T>A (PDYN) MANE Select	NP_077722.1:n.-214T>A
NM_001190898.3:c.-211T>A (PDYN)	NP_001177827.1:n.-211T>A