Canonical Allele Identifier: CA2555402024

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.12800493_12800494insGATT , CM000681.2:g.12800493_12800494insGATT GRCh38
NC_000019.9:g.12911307_12911308insGATT , CM000681.1:g.12911307_12911308insGATT GRCh37
NC_000019.8:g.12772307_12772308insGATT NCBI36
NG_029901.1:g.6387_6388insAATC

Transcript Alleles

HGVS Amino-acid change
ENST00000301522.3:c.258-195_258-194insAATC (PRDX2) MANE Select ENSP00000301522.2:n.258-195_258-194insAAT...
ENST00000301522.2:c.258-195_258-194insAATC (PRDX2) ENSP00000301522.2:n.258-195_258-194insAAT...
ENST00000334482.9:c.258-195_258-194insAATC (PRDX2) ENSP00000334063.5:n.258-195_258-194insAAT...
ENST00000466174.5:n.738_739insAATC (PRDX2)
ENST00000477555.1:n.316-195_316-194insAATC (PRDX2)
ENST00000589765.1:n.41+24684_41+24685insAATC (HOOK2)
NM_005809.5:c.258-195_258-194insAATC (PRDX2) NP_005800.3:n.258-195_258-194insAATC
NM_005809.6:c.258-195_258-194insAATC (PRDX2) MANE Select NP_005800.3:n.258-195_258-194insAATC