Canonical Allele Identifier: CA5714898
Community Standard Title: NM_006793.5(PRDX3):c.425C>G (p.Ala142Gly)
Gene: PRDX3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.119173759G>C , CM000672.2:g.119173759G>C GRCh38
NC_000010.10:g.120933271G>C , CM000672.1:g.120933271G>C GRCh37
NC_000010.9:g.120923261G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_006793.5:c.425C>G MANE Select NP_006784.1:p.Ala142Gly
ENST00000298510.4:c.425C>G MANE Select ENSP00000298510.2:p.Ala142Gly
NM_001302272.1:c.425C>G NP_001289201.1:p.Ala142Gly
NM_001302272.2:c.425C>G NP_001289201.1:p.Ala142Gly
NM_006793.4:c.425C>G NP_006784.1:p.Ala142Gly
NR_126102.1:n.367C>G
NR_126102.2:n.314C>G
NR_126103.1:n.225C>G
NR_126103.2:n.172C>G
NR_126105.1:n.217C>G
NR_126105.2:n.164C>G
NR_126106.1:n.123+3383C>G
NR_126106.2:n.70+3383C>G
ENST00000298510.3:c.425C>G ENSP00000298510.2:p.Ala142Gly
ENST00000463322.1:n.436C>G