Canonical Allele Identifier: CA2323577442

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.12800501_12800504delinsGCTC , CM000681.2:g.12800501_12800504delinsGCTC GRCh38
NC_000019.9:g.12911315_12911318delinsGCTC , CM000681.1:g.12911315_12911318delinsGCTC GRCh37
NC_000019.8:g.12772315_12772318delinsGCTC NCBI36
NG_029901.1:g.6377_6380delinsGAGC

Transcript Alleles

HGVS Amino-acid change
ENST00000301522.3:c.258-205_258-202delinsGAGC (PRDX2) MANE Select ENSP00000301522.2:n.258-205_258-202delinsGAGC
ENST00000301522.2:c.258-205_258-202delinsGAGC (PRDX2) ENSP00000301522.2:n.258-205_258-202delinsGAGC
ENST00000334482.9:c.258-205_258-202delinsGAGC (PRDX2) ENSP00000334063.5:n.258-205_258-202delinsGAGC
ENST00000466174.5:n.728_731delinsGAGC (PRDX2)
ENST00000477555.1:n.316-205_316-202delinsGAGC (PRDX2)
ENST00000589765.1:n.41+24674_41+24677delinsGAGC (HOOK2)
NM_005809.5:c.258-205_258-202delinsGAGC (PRDX2) NP_005800.3:n.258-205_258-202delinsGAGC
NM_005809.6:c.258-205_258-202delinsGAGC (PRDX2) MANE Select NP_005800.3:n.258-205_258-202delinsGAGC