Canonical Allele Identifier: CA10643526

Gene: PDYN PDYN-AS1

Linked Data

• ClinVar Variation Id: 337813
• ClinVar RCV Id: RCV000346631 ; RCV003437076
• dbSNP Id: rs752953257
• gnomAD v2: 20-1959898-C-T
• gnomAD v3: 20-1979252-C-T
• gnomAD v4: 20-1979252-C-T
• MyVariant Identifiers: chr20:g.1959898C>T (hg19) ; chr20:g.1979252C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.1979252C>T , CM000682.2:g.1979252C>T	GRCh38
NC_000020.10:g.1959898C>T , CM000682.1:g.1959898C>T	GRCh37
NC_000020.9:g.1907898C>T	NCBI36
NG_028027.1:g.19994G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000217305.3:c.*1071G>A (PDYN) MANE Select	ENSP00000217305.2:n.*1071G>A
ENST00000217305.2:c.*1071G>A (PDYN)	ENSP00000217305.2:n.*1071G>A
ENST00000539905.5:c.*1071G>A (PDYN)	ENSP00000440185.1:n.*1071G>A
ENST00000540134.5:c.*1071G>A (PDYN)	ENSP00000442259.1:n.*1071G>A
NM_001190892.1:c.*1071G>A (PDYN)	NP_001177821.1:n.*1071G>A
NM_001190898.2:c.*1071G>A (PDYN)	NP_001177827.1:n.*1071G>A
NM_001190899.2:c.*1071G>A (PDYN)	NP_001177828.1:n.*1071G>A
NM_001190900.1:c.*1071G>A (PDYN)	NP_001177829.1:n.*1071G>A
NM_024411.4:c.*1071G>A (PDYN)	NP_077722.1:n.*1071G>A
XM_011529244.1:c.*1071G>A (PDYN)	XP_011527546.1:n.*1071G>A
XM_011529245.1:c.*1071G>A (PDYN)	XP_011527547.1:n.*1071G>A
XM_011529246.1:c.*1071G>A (PDYN)	XP_011527548.1:n.*1071G>A
XM_011529247.1:c.*1071G>A (PDYN)	XP_011527549.1:n.*1071G>A
XM_011529248.1:c.*1071G>A (PDYN)	XP_011527550.1:n.*1071G>A
XM_011529249.1:c.*1071G>A (PDYN)	XP_011527551.1:n.*1071G>A
XM_011529250.1:c.*1071G>A (PDYN)	XP_011527552.1:n.*1071G>A
XR_244229.1:n.1216+12909C>T (PDYN-AS1)
NR_134520.1:n.1252+12909C>T (PDYN-AS1)
XM_011529246.2:c.*1071G>A (PDYN)	XP_011527548.1:n.*1071G>A
XM_011529249.2:c.*1071G>A (PDYN)	XP_011527551.1:n.*1071G>A
XM_011529250.2:c.*1071G>A (PDYN)	XP_011527552.1:n.*1071G>A
XM_017027878.1:c.*1071G>A (PDYN)	XP_016883367.1:n.*1071G>A
NM_024411.5:c.*1071G>A (PDYN) MANE Select	NP_077722.1:n.*1071G>A
NM_001190898.3:c.*1071G>A (PDYN)	NP_001177827.1:n.*1071G>A