Canonical Allele Identifier: CA378286181
Community Standard Title: NM_006793.5(PRDX3):c.489C>G (p.Asp163Glu)
Gene: PRDX3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.119172444G>C , CM000672.2:g.119172444G>C GRCh38
NC_000010.10:g.120931956G>C , CM000672.1:g.120931956G>C GRCh37
NC_000010.9:g.120921946G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_006793.5:c.489C>G MANE Select NP_006784.1:p.Asp163Glu
ENST00000298510.4:c.489C>G MANE Select ENSP00000298510.2:p.Asp163Glu
NM_001302272.1:c.489C>G NP_001289201.1:p.Asp163Glu
NM_001302272.2:c.489C>G NP_001289201.1:p.Asp163Glu
NM_006793.4:c.489C>G NP_006784.1:p.Asp163Glu
NR_126102.1:n.431C>G
NR_126102.2:n.378C>G
NR_126103.1:n.289C>G
NR_126103.2:n.236C>G
NR_126105.1:n.281C>G
NR_126105.2:n.228C>G
NR_126106.1:n.124-3131C>G
NR_126106.2:n.71-3131C>G
ENST00000298510.3:c.489C>G ENSP00000298510.2:p.Asp163Glu