Canonical Allele Identifier: CA2345900687

Gene: PDYN PDYN-AS1

Linked Data

• dbSNP Id: rs1988561385

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.1994021A>C , CM000682.2:g.1994021A>C	GRCh38
NC_000020.10:g.1974667A>C , CM000682.1:g.1974667A>C	GRCh37
NC_000020.9:g.1922667A>C	NCBI36
NG_028027.1:g.5225T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000217305.3:c.-190T>G (PDYN) MANE Select	ENSP00000217305.2:n.-190T>G
ENST00000650874.1:c.-130T>G (PDYN)	ENSP00000498438.1:n.-130T>G
ENST00000651882.1:c.-187T>G (PDYN)	ENSP00000498752.1:n.-187T>G
ENST00000217305.2:c.-190T>G (PDYN)	ENSP00000217305.2:n.-190T>G
ENST00000539905.5:c.-130T>G (PDYN)	ENSP00000440185.1:n.-130T>G
NM_001190898.2:c.-187T>G (PDYN)	NP_001177827.1:n.-187T>G
NM_001190899.2:c.-130T>G (PDYN)	NP_001177828.1:n.-130T>G
NM_024411.4:c.-190T>G (PDYN)	NP_077722.1:n.-190T>G
XR_244229.1:n.1217-12911A>C (PDYN-AS1)
NR_134520.1:n.1253-12911A>C (PDYN-AS1)
NM_024411.5:c.-190T>G (PDYN) MANE Select	NP_077722.1:n.-190T>G
NM_001190898.3:c.-187T>G (PDYN)	NP_001177827.1:n.-187T>G