Canonical Allele Identifier: CA21837045
Gene: PRDX1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.45515436G>A , CM000663.2:g.45515436G>A GRCh38
NC_000001.10:g.45981108G>A , CM000663.1:g.45981108G>A GRCh37
NC_000001.9:g.45753695G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000319248.13:c.260+218C>T MANE Select ENSP00000361152.5:n.260+218C>T
ENST00000424390.2:c.260+218C>T ENSP00000389047.2:n.260+218C>T
ENST00000447184.6:c.260+218C>T ENSP00000407034.2:n.260+218C>T
ENST00000676549.1:c.260+218C>T ENSP00000503140.1:n.260+218C>T
ENST00000262746.5:c.260+218C>T ENSP00000262746.1:n.260+218C>T
ENST00000319248.12:c.260+218C>T ENSP00000361152.5:n.260+218C>T
ENST00000372079.1:c.55-541C>T ENSP00000361150.1:n.55-541C>T
ENST00000424390.1:c.260+218C>T ENSP00000389047.1:n.260+218C>T
ENST00000447184.5:c.260+218C>T ENSP00000407034.1:n.260+218C>T
NM_001202431.1:c.260+218C>T NP_001189360.1:n.260+218C>T
NM_002574.3:c.260+218C>T NP_002565.1:n.260+218C>T
NM_181696.2:c.260+218C>T NP_859047.1:n.260+218C>T
NM_181697.2:c.260+218C>T NP_859048.1:n.260+218C>T
NM_181697.3:c.260+218C>T MANE Select NP_859048.1:n.260+218C>T
NM_001202431.2:c.260+218C>T NP_001189360.1:n.260+218C>T
NM_002574.4:c.260+218C>T NP_002565.1:n.260+218C>T
NM_181696.3:c.260+218C>T NP_859047.1:n.260+218C>T