Canonical Allele Identifier: CA3214606
Gene: PRDM9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.23522303G>A , CM000667.2:g.23522303G>A GRCh38
NC_000005.9:g.23522412G>A , CM000667.1:g.23522412G>A GRCh37
NC_000005.8:g.23558169G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000502755.6:c.509-1G>A ENSP00000425471.2:n.509-1G>A
ENST00000296682.4:c.509-1G>A MANE Select ENSP00000296682.4:n.509-1G>A
ENST00000296682.3:c.509-1G>A ENSP00000296682.3:n.509-1G>A
ENST00000635252.1:c.332-1G>A ENSP00000489227.1:n.332-1G>A
NM_020227.2:c.509-1G>A NP_064612.2:n.509-1G>A
NM_020227.3:c.509-1G>A NP_064612.2:n.509-1G>A
NM_001376900.1:c.509-1G>A NP_001363829.1:n.509-1G>A
NM_020227.4:c.509-1G>A MANE Select NP_064612.2:n.509-1G>A