Canonical Allele Identifier: CA3214744
Gene: PRDM9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.23523299G>A , CM000667.2:g.23523299G>A GRCh38
NC_000005.9:g.23523408G>A , CM000667.1:g.23523408G>A GRCh37
NC_000005.8:g.23559165G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000502755.6:c.891G>A ENSP00000425471.2:p.Lys297=
ENST00000296682.4:c.891G>A MANE Select ENSP00000296682.4:p.Lys297=
ENST00000296682.3:c.891G>A ENSP00000296682.3:p.Lys297=
ENST00000635252.1:c.714G>A ENSP00000489227.1:p.Lys238=
NM_020227.2:c.891G>A NP_064612.2:p.Lys297=
NM_020227.3:c.891G>A NP_064612.2:p.Lys297=
NM_001376900.1:c.891G>A NP_001363829.1:p.Lys297=
NM_020227.4:c.891G>A MANE Select NP_064612.2:p.Lys297=