Canonical Allele Identifier: CA2651618134

Gene: PDYN PDYN-AS1

Linked Data

• gnomAD v4: 20-1994028-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.1994028G>T , CM000682.2:g.1994028G>T	GRCh38
NC_000020.10:g.1974674G>T , CM000682.1:g.1974674G>T	GRCh37
NC_000020.9:g.1922674G>T	NCBI36
NG_028027.1:g.5218C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000217305.3:c.-197C>A (PDYN) MANE Select	ENSP00000217305.2:n.-197C>A
ENST00000650874.1:c.-137C>A (PDYN)	ENSP00000498438.1:n.-137C>A
ENST00000651882.1:c.-194C>A (PDYN)	ENSP00000498752.1:n.-194C>A
ENST00000217305.2:c.-197C>A (PDYN)	ENSP00000217305.2:n.-197C>A
ENST00000539905.5:c.-137C>A (PDYN)	ENSP00000440185.1:n.-137C>A
NM_001190898.2:c.-194C>A (PDYN)	NP_001177827.1:n.-194C>A
NM_001190899.2:c.-137C>A (PDYN)	NP_001177828.1:n.-137C>A
NM_024411.4:c.-197C>A (PDYN)	NP_077722.1:n.-197C>A
XR_244229.1:n.1217-12904G>T (PDYN-AS1)
NR_134520.1:n.1253-12904G>T (PDYN-AS1)
NM_024411.5:c.-197C>A (PDYN) MANE Select	NP_077722.1:n.-197C>A
NM_001190898.3:c.-194C>A (PDYN)	NP_001177827.1:n.-194C>A