Canonical Allele Identifier: CA741924355

Gene: PDYN PDYN-AS1

Linked Data

• dbSNP Id: rs1263335412
• gnomAD v3: 20-1994043-A-C
• gnomAD v4: 20-1994043-A-C
• MyVariant Identifiers: chr20:g.1974689A>C (hg19) ; chr20:g.1994043A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.1994043A>C , CM000682.2:g.1994043A>C	GRCh38
NC_000020.10:g.1974689A>C , CM000682.1:g.1974689A>C	GRCh37
NC_000020.9:g.1922689A>C	NCBI36
NG_028027.1:g.5203T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000217305.3:c.-212T>G (PDYN) MANE Select	ENSP00000217305.2:n.-212T>G
ENST00000650874.1:c.-152T>G (PDYN)	ENSP00000498438.1:n.-152T>G
ENST00000651882.1:c.-209T>G (PDYN)	ENSP00000498752.1:n.-209T>G
ENST00000217305.2:c.-212T>G (PDYN)	ENSP00000217305.2:n.-212T>G
ENST00000539905.5:c.-152T>G (PDYN)	ENSP00000440185.1:n.-152T>G
NM_001190898.2:c.-209T>G (PDYN)	NP_001177827.1:n.-209T>G
NM_001190899.2:c.-152T>G (PDYN)	NP_001177828.1:n.-152T>G
NM_024411.4:c.-212T>G (PDYN)	NP_077722.1:n.-212T>G
XR_244229.1:n.1217-12889A>C (PDYN-AS1)
NR_134520.1:n.1253-12889A>C (PDYN-AS1)
NM_024411.5:c.-212T>G (PDYN) MANE Select	NP_077722.1:n.-212T>G
NM_001190898.3:c.-209T>G (PDYN)	NP_001177827.1:n.-209T>G