Canonical Allele Identifier: CA2582752928

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.12800388G>T , CM000681.2:g.12800388G>T GRCh38
NC_000019.9:g.12911202G>T , CM000681.1:g.12911202G>T GRCh37
NC_000019.8:g.12772202G>T NCBI36
NG_029901.1:g.6493C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000301522.3:c.258-89C>A (PRDX2) MANE Select ENSP00000301522.2:n.258-89C>A
ENST00000301522.2:c.258-89C>A (PRDX2) ENSP00000301522.2:n.258-89C>A
ENST00000334482.9:c.258-89C>A (PRDX2) ENSP00000334063.5:n.258-89C>A
ENST00000466174.5:n.844C>A (PRDX2)
ENST00000477555.1:n.316-89C>A (PRDX2)
ENST00000478908.1:n.74C>A (PRDX2)
ENST00000589765.1:n.41+24790C>A (HOOK2)
NM_005809.5:c.258-89C>A (PRDX2) NP_005800.3:n.258-89C>A
NM_005809.6:c.258-89C>A (PRDX2) MANE Select NP_005800.3:n.258-89C>A