Canonical Allele Identifier: CA214193074
Community Standard Title: NM_006793.5(PRDX3):c.539G>A (p.Gly180Asp)
Gene: PRDX3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.119172394C>T , CM000672.2:g.119172394C>T GRCh38
NC_000010.10:g.120931906C>T , CM000672.1:g.120931906C>T GRCh37
NC_000010.9:g.120921896C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_006793.5:c.539G>A MANE Select NP_006784.1:p.Gly180Asp
ENST00000298510.4:c.539G>A MANE Select ENSP00000298510.2:p.Gly180Asp
NM_001302272.1:c.539G>A NP_001289201.1:p.Gly180Asp
NM_001302272.2:c.539G>A NP_001289201.1:p.Gly180Asp
NM_006793.4:c.539G>A NP_006784.1:p.Gly180Asp
NR_126102.1:n.481G>A
NR_126102.2:n.428G>A
NR_126103.1:n.339G>A
NR_126103.2:n.286G>A
NR_126105.1:n.331G>A
NR_126105.2:n.278G>A
NR_126106.1:n.124-3081G>A
NR_126106.2:n.71-3081G>A
ENST00000298510.3:c.539G>A ENSP00000298510.2:p.Gly180Asp