Canonical Allele Identifier: CA2345893858
Gene: PDYN HGNC NCBI
PDYN-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.1979238G= , CM000682.2:g.1979238G= GRCh38
NC_000020.10:g.1959884G= , CM000682.1:g.1959884G= GRCh37
NC_000020.9:g.1907884G= NCBI36
NG_028027.1:g.20008C=

Transcript Alleles

HGVS Amino-acid change
ENST00000217305.3:c.*1085C= (PDYN) MANE Select ENSP00000217305.2:n.*1085C=
ENST00000217305.2:c.*1085C= (PDYN) ENSP00000217305.2:n.*1085C=
ENST00000539905.5:c.*1085C= (PDYN) ENSP00000440185.1:n.*1085C=
ENST00000540134.5:c.*1085C= (PDYN) ENSP00000442259.1:n.*1085C=
NM_001190892.1:c.*1085C= (PDYN) NP_001177821.1:n.*1085C=
NM_001190898.2:c.*1085C= (PDYN) NP_001177827.1:n.*1085C=
NM_001190899.2:c.*1085C= (PDYN) NP_001177828.1:n.*1085C=
NM_001190900.1:c.*1085C= (PDYN) NP_001177829.1:n.*1085C=
NM_024411.4:c.*1085C= (PDYN) NP_077722.1:n.*1085C=
XM_011529244.1:c.*1085C= (PDYN) XP_011527546.1:n.*1085C=
XM_011529245.1:c.*1085C= (PDYN) XP_011527547.1:n.*1085C=
XM_011529246.1:c.*1085C= (PDYN) XP_011527548.1:n.*1085C=
XM_011529247.1:c.*1085C= (PDYN) XP_011527549.1:n.*1085C=
XM_011529248.1:c.*1085C= (PDYN) XP_011527550.1:n.*1085C=
XM_011529249.1:c.*1085C= (PDYN) XP_011527551.1:n.*1085C=
XM_011529250.1:c.*1085C= (PDYN) XP_011527552.1:n.*1085C=
XR_244229.1:n.1216+12895G= (PDYN-AS1)
NR_134520.1:n.1252+12895G= (PDYN-AS1)
XM_011529246.2:c.*1085C= (PDYN) XP_011527548.1:n.*1085C=
XM_011529249.2:c.*1085C= (PDYN) XP_011527551.1:n.*1085C=
XM_011529250.2:c.*1085C= (PDYN) XP_011527552.1:n.*1085C=
XM_017027878.1:c.*1085C= (PDYN) XP_016883367.1:n.*1085C=
NM_024411.5:c.*1085C= (PDYN) MANE Select NP_077722.1:n.*1085C=
NM_001190898.3:c.*1085C= (PDYN) NP_001177827.1:n.*1085C=