Canonical Allele Identifier: CA2323577445

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.12800505C= , CM000681.2:g.12800505C= GRCh38
NC_000019.9:g.12911319C= , CM000681.1:g.12911319C= GRCh37
NC_000019.8:g.12772319C= NCBI36
NG_029901.1:g.6376G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000301522.3:c.258-206G= (PRDX2) MANE Select ENSP00000301522.2:n.258-206G=
ENST00000301522.2:c.258-206G= (PRDX2) ENSP00000301522.2:n.258-206G=
ENST00000334482.9:c.258-206G= (PRDX2) ENSP00000334063.5:n.258-206G=
ENST00000466174.5:n.727G= (PRDX2)
ENST00000477555.1:n.316-206G= (PRDX2)
ENST00000589765.1:n.41+24673G= (HOOK2)
NM_005809.5:c.258-206G= (PRDX2) NP_005800.3:n.258-206G=
NM_005809.6:c.258-206G= (PRDX2) MANE Select NP_005800.3:n.258-206G=