Canonical Allele Identifier: CA310400272

Gene: PDYN PDYN-AS1

Linked Data

• dbSNP Id: rs998406161
• gnomAD v3: 20-1994033-G-A
• gnomAD v4: 20-1994033-G-A
• MyVariant Identifiers: chr20:g.1974679G>A (hg19) ; chr20:g.1994033G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.1994033G>A , CM000682.2:g.1994033G>A	GRCh38
NC_000020.10:g.1974679G>A , CM000682.1:g.1974679G>A	GRCh37
NC_000020.9:g.1922679G>A	NCBI36
NG_028027.1:g.5213C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000217305.3:c.-202C>T (PDYN) MANE Select	ENSP00000217305.2:n.-202C>T
ENST00000650874.1:c.-142C>T (PDYN)	ENSP00000498438.1:n.-142C>T
ENST00000651882.1:c.-199C>T (PDYN)	ENSP00000498752.1:n.-199C>T
ENST00000217305.2:c.-202C>T (PDYN)	ENSP00000217305.2:n.-202C>T
ENST00000539905.5:c.-142C>T (PDYN)	ENSP00000440185.1:n.-142C>T
NM_001190898.2:c.-199C>T (PDYN)	NP_001177827.1:n.-199C>T
NM_001190899.2:c.-142C>T (PDYN)	NP_001177828.1:n.-142C>T
NM_024411.4:c.-202C>T (PDYN)	NP_077722.1:n.-202C>T
XR_244229.1:n.1217-12899G>A (PDYN-AS1)
NR_134520.1:n.1253-12899G>A (PDYN-AS1)
NM_024411.5:c.-202C>T (PDYN) MANE Select	NP_077722.1:n.-202C>T
NM_001190898.3:c.-199C>T (PDYN)	NP_001177827.1:n.-199C>T