Canonical Allele Identifier: CA2651618143

Gene: PDYN PDYN-AS1

Linked Data

• gnomAD v4: 20-1994037-A-T

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.1994037A>T , CM000682.2:g.1994037A>T	GRCh38
NC_000020.10:g.1974683A>T , CM000682.1:g.1974683A>T	GRCh37
NC_000020.9:g.1922683A>T	NCBI36
NG_028027.1:g.5209T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000217305.3:c.-206T>A (PDYN) MANE Select	ENSP00000217305.2:n.-206T>A
ENST00000650874.1:c.-146T>A (PDYN)	ENSP00000498438.1:n.-146T>A
ENST00000651882.1:c.-203T>A (PDYN)	ENSP00000498752.1:n.-203T>A
ENST00000217305.2:c.-206T>A (PDYN)	ENSP00000217305.2:n.-206T>A
ENST00000539905.5:c.-146T>A (PDYN)	ENSP00000440185.1:n.-146T>A
NM_001190898.2:c.-203T>A (PDYN)	NP_001177827.1:n.-203T>A
NM_001190899.2:c.-146T>A (PDYN)	NP_001177828.1:n.-146T>A
NM_024411.4:c.-206T>A (PDYN)	NP_077722.1:n.-206T>A
XR_244229.1:n.1217-12895A>T (PDYN-AS1)
NR_134520.1:n.1253-12895A>T (PDYN-AS1)
NM_024411.5:c.-206T>A (PDYN) MANE Select	NP_077722.1:n.-206T>A
NM_001190898.3:c.-203T>A (PDYN)	NP_001177827.1:n.-203T>A