Canonical Allele Identifier: CA2578276501
Gene: PRDM9 HGNC NCBI

Linked Data

gnomAD v4: 5-23508944-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.23508944C>T , CM000667.2:g.23508944C>T GRCh38
NC_000005.9:g.23509053C>T , CM000667.1:g.23509053C>T GRCh37
NC_000005.8:g.23544810C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000502755.6:c.-84-6C>T ENSP00000425471.2:n.-84-6C>T
ENST00000296682.4:c.-84-6C>T MANE Select ENSP00000296682.4:n.-84-6C>T
ENST00000296682.3:c.-84-6C>T ENSP00000296682.3:n.-84-6C>T
ENST00000502755.5:c.-84-6C>T ENSP00000425471.1:n.-84-6C>T
ENST00000635252.1:c.17-976C>T ENSP00000489227.1:n.17-976C>T
NM_020227.2:c.-84-6C>T NP_064612.2:n.-84-6C>T
NM_020227.3:c.-84-6C>T NP_064612.2:n.-84-6C>T
NM_001376900.1:c.-84-6C>T NP_001363829.1:n.-84-6C>T
NM_020227.4:c.-84-6C>T MANE Select NP_064612.2:n.-84-6C>T