Canonical Allele Identifier: CA2578276502
Gene: PRDM9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.23508947C>A , CM000667.2:g.23508947C>A GRCh38
NC_000005.9:g.23509056C>A , CM000667.1:g.23509056C>A GRCh37
NC_000005.8:g.23544813C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000502755.6:c.-84-3C>A ENSP00000425471.2:n.-84-3C>A
ENST00000296682.4:c.-84-3C>A MANE Select ENSP00000296682.4:n.-84-3C>A
ENST00000296682.3:c.-84-3C>A ENSP00000296682.3:n.-84-3C>A
ENST00000502755.5:c.-84-3C>A ENSP00000425471.1:n.-84-3C>A
ENST00000635252.1:c.17-973C>A ENSP00000489227.1:n.17-973C>A
NM_020227.2:c.-84-3C>A NP_064612.2:n.-84-3C>A
NM_020227.3:c.-84-3C>A NP_064612.2:n.-84-3C>A
NM_001376900.1:c.-84-3C>A NP_001363829.1:n.-84-3C>A
NM_020227.4:c.-84-3C>A MANE Select NP_064612.2:n.-84-3C>A