Canonical Allele Identifier: CA1533058924
Gene: PRDM9 HGNC NCBI
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Genomic Alleles

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

Transcript Alleles

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