Canonical Allele Identifier: CA2345898536

Gene: PDYN PDYN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.1989326C= , CM000682.2:g.1989326C=	GRCh38
NC_000020.10:g.1969972C= , CM000682.1:g.1969972C=	GRCh37
NC_000020.9:g.1917972C=	NCBI36
NG_028027.1:g.9920G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000217305.3:c.-20+3258G= (PDYN) MANE Select	ENSP00000217305.2:n.-20+3258G=
ENST00000650824.1:c.-20+3258G= (PDYN)	ENSP00000499095.1:n.-20+3258G=
ENST00000650874.1:c.-20+4585G= (PDYN)	ENSP00000498438.1:n.-20+4585G=
ENST00000650937.1:c.-20+3258G= (PDYN)	ENSP00000498947.1:n.-20+3258G=
ENST00000651882.1:c.-17+3258G= (PDYN)	ENSP00000498752.1:n.-17+3258G=
ENST00000217305.2:c.-20+3258G= (PDYN)	ENSP00000217305.2:n.-20+3258G=
ENST00000539905.5:c.-20+4585G= (PDYN)	ENSP00000440185.1:n.-20+4585G=
ENST00000540134.5:c.-20+3258G= (PDYN)	ENSP00000442259.1:n.-20+3258G=
NM_001190892.1:c.-20+3258G= (PDYN)	NP_001177821.1:n.-20+3258G=
NM_001190898.2:c.-17+3258G= (PDYN)	NP_001177827.1:n.-17+3258G=
NM_001190899.2:c.-20+4585G= (PDYN)	NP_001177828.1:n.-20+4585G=
NM_001190900.1:c.-20+3258G= (PDYN)	NP_001177829.1:n.-20+3258G=
NM_024411.4:c.-20+3258G= (PDYN)	NP_077722.1:n.-20+3258G=
XR_244229.1:n.1217-17606C= (PDYN-AS1)
NR_134520.1:n.1253-17606C= (PDYN-AS1)
NM_024411.5:c.-20+3258G= (PDYN) MANE Select	NP_077722.1:n.-20+3258G=
NM_001190898.3:c.-17+3258G= (PDYN)	NP_001177827.1:n.-17+3258G=