Canonical Allele Identifier: CA741921731

Gene: PDYN PDYN-AS1

Linked Data

• dbSNP Id: rs1356577645
• gnomAD v3: 20-1989305-T-C
• gnomAD v4: 20-1989305-T-C
• MyVariant Identifiers: chr20:g.1969951T>C (hg19) ; chr20:g.1989305T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.1989305T>C , CM000682.2:g.1989305T>C	GRCh38
NC_000020.10:g.1969951T>C , CM000682.1:g.1969951T>C	GRCh37
NC_000020.9:g.1917951T>C	NCBI36
NG_028027.1:g.9941A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000217305.3:c.-20+3279A>G (PDYN) MANE Select	ENSP00000217305.2:n.-20+3279A>G
ENST00000650824.1:c.-20+3279A>G (PDYN)	ENSP00000499095.1:n.-20+3279A>G
ENST00000650874.1:c.-20+4606A>G (PDYN)	ENSP00000498438.1:n.-20+4606A>G
ENST00000650937.1:c.-20+3279A>G (PDYN)	ENSP00000498947.1:n.-20+3279A>G
ENST00000651882.1:c.-17+3279A>G (PDYN)	ENSP00000498752.1:n.-17+3279A>G
ENST00000217305.2:c.-20+3279A>G (PDYN)	ENSP00000217305.2:n.-20+3279A>G
ENST00000539905.5:c.-20+4606A>G (PDYN)	ENSP00000440185.1:n.-20+4606A>G
ENST00000540134.5:c.-20+3279A>G (PDYN)	ENSP00000442259.1:n.-20+3279A>G
NM_001190892.1:c.-20+3279A>G (PDYN)	NP_001177821.1:n.-20+3279A>G
NM_001190898.2:c.-17+3279A>G (PDYN)	NP_001177827.1:n.-17+3279A>G
NM_001190899.2:c.-20+4606A>G (PDYN)	NP_001177828.1:n.-20+4606A>G
NM_001190900.1:c.-20+3279A>G (PDYN)	NP_001177829.1:n.-20+3279A>G
NM_024411.4:c.-20+3279A>G (PDYN)	NP_077722.1:n.-20+3279A>G
XR_244229.1:n.1217-17627T>C (PDYN-AS1)
NR_134520.1:n.1253-17627T>C (PDYN-AS1)
NM_024411.5:c.-20+3279A>G (PDYN) MANE Select	NP_077722.1:n.-20+3279A>G
NM_001190898.3:c.-17+3279A>G (PDYN)	NP_001177827.1:n.-17+3279A>G