Canonical Allele Identifier: CA14831935
Gene: PDYN HGNC NCBI
PDYN-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs2281285
gnomAD v2: 20-1972460-T-C
gnomAD v3: 20-1991814-T-C
gnomAD v4: 20-1991814-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.1991814T>C , CM000682.2:g.1991814T>C GRCh38
NC_000020.10:g.1972460T>C , CM000682.1:g.1972460T>C GRCh37
NC_000020.9:g.1920460T>C NCBI36
NG_028027.1:g.7432A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000217305.3:c.-20+770A>G (PDYN) MANE Select ENSP00000217305.2:n.-20+770A>G
ENST00000650824.1:c.-20+770A>G (PDYN) ENSP00000499095.1:n.-20+770A>G
ENST00000650874.1:c.-20+2097A>G (PDYN) ENSP00000498438.1:n.-20+2097A>G
ENST00000650937.1:c.-20+770A>G (PDYN) ENSP00000498947.1:n.-20+770A>G
ENST00000651882.1:c.-17+770A>G (PDYN) ENSP00000498752.1:n.-17+770A>G
ENST00000217305.2:c.-20+770A>G (PDYN) ENSP00000217305.2:n.-20+770A>G
ENST00000539905.5:c.-20+2097A>G (PDYN) ENSP00000440185.1:n.-20+2097A>G
ENST00000540134.5:c.-20+770A>G (PDYN) ENSP00000442259.1:n.-20+770A>G
NM_001190892.1:c.-20+770A>G (PDYN) NP_001177821.1:n.-20+770A>G
NM_001190898.2:c.-17+770A>G (PDYN) NP_001177827.1:n.-17+770A>G
NM_001190899.2:c.-20+2097A>G (PDYN) NP_001177828.1:n.-20+2097A>G
NM_001190900.1:c.-20+770A>G (PDYN) NP_001177829.1:n.-20+770A>G
NM_024411.4:c.-20+770A>G (PDYN) NP_077722.1:n.-20+770A>G
XR_244229.1:n.1217-15118T>C (PDYN-AS1)
NR_134520.1:n.1253-15118T>C (PDYN-AS1)
NM_024411.5:c.-20+770A>G (PDYN) MANE Select NP_077722.1:n.-20+770A>G
NM_001190898.3:c.-17+770A>G (PDYN) NP_001177827.1:n.-17+770A>G