Canonical Allele Identifier: CA741913788

Gene: PDYN PDYN-AS1

Linked Data

• dbSNP Id: rs1179784423
• gnomAD v3: 20-1994046-G-A
• gnomAD v4: 20-1994046-G-A
• MyVariant Identifiers: chr20:g.1974692G>A (hg19) ; chr20:g.1994046G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.1994046G>A , CM000682.2:g.1994046G>A	GRCh38
NC_000020.10:g.1974692G>A , CM000682.1:g.1974692G>A	GRCh37
NC_000020.9:g.1922692G>A	NCBI36
NG_028027.1:g.5200C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000217305.3:c.-215C>T (PDYN) MANE Select	ENSP00000217305.2:n.-215C>T
ENST00000650874.1:c.-155C>T (PDYN)	ENSP00000498438.1:n.-155C>T
ENST00000651882.1:c.-212C>T (PDYN)	ENSP00000498752.1:n.-212C>T
ENST00000217305.2:c.-215C>T (PDYN)	ENSP00000217305.2:n.-215C>T
ENST00000539905.5:c.-155C>T (PDYN)	ENSP00000440185.1:n.-155C>T
NM_001190898.2:c.-212C>T (PDYN)	NP_001177827.1:n.-212C>T
NM_001190899.2:c.-155C>T (PDYN)	NP_001177828.1:n.-155C>T
NM_024411.4:c.-215C>T (PDYN)	NP_077722.1:n.-215C>T
XR_244229.1:n.1217-12886G>A (PDYN-AS1)
NR_134520.1:n.1253-12886G>A (PDYN-AS1)
NM_024411.5:c.-215C>T (PDYN) MANE Select	NP_077722.1:n.-215C>T
NM_001190898.3:c.-212C>T (PDYN)	NP_001177827.1:n.-212C>T