Canonical Allele Identifier: CA2651618131

Gene: PDYN PDYN-AS1

Linked Data

• gnomAD v4: 20-1994026-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.1994026C>A , CM000682.2:g.1994026C>A	GRCh38
NC_000020.10:g.1974672C>A , CM000682.1:g.1974672C>A	GRCh37
NC_000020.9:g.1922672C>A	NCBI36
NG_028027.1:g.5220G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000217305.3:c.-195G>T (PDYN) MANE Select	ENSP00000217305.2:n.-195G>T
ENST00000650874.1:c.-135G>T (PDYN)	ENSP00000498438.1:n.-135G>T
ENST00000651882.1:c.-192G>T (PDYN)	ENSP00000498752.1:n.-192G>T
ENST00000217305.2:c.-195G>T (PDYN)	ENSP00000217305.2:n.-195G>T
ENST00000539905.5:c.-135G>T (PDYN)	ENSP00000440185.1:n.-135G>T
NM_001190898.2:c.-192G>T (PDYN)	NP_001177827.1:n.-192G>T
NM_001190899.2:c.-135G>T (PDYN)	NP_001177828.1:n.-135G>T
NM_024411.4:c.-195G>T (PDYN)	NP_077722.1:n.-195G>T
XR_244229.1:n.1217-12906C>A (PDYN-AS1)
NR_134520.1:n.1253-12906C>A (PDYN-AS1)
NM_024411.5:c.-195G>T (PDYN) MANE Select	NP_077722.1:n.-195G>T
NM_001190898.3:c.-192G>T (PDYN)	NP_001177827.1:n.-192G>T