Canonical Allele Identifier: CA443558072

Gene: PRDM9

Linked Data

• MyVariant Identifiers: chr5:g.23509154A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.23509045A>G , CM000667.2:g.23509045A>G	GRCh38
NC_000005.9:g.23509154A>G , CM000667.1:g.23509154A>G	GRCh37
NC_000005.8:g.23544911A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502755.6:c.12A>G	ENSP00000425471.2:p.Glu4=
ENST00000296682.4:c.12A>G MANE Select	ENSP00000296682.4:p.Glu4=
ENST00000296682.3:c.12A>G	ENSP00000296682.3:p.Glu4=
ENST00000502755.5:c.12A>G	ENSP00000425471.1:p.Glu4=
ENST00000635252.1:c.17-875A>G	ENSP00000489227.1:n.17-875A>G
NM_020227.2:c.12A>G	NP_064612.2:p.Glu4=
NM_020227.3:c.12A>G	NP_064612.2:p.Glu4=
NM_001376900.1:c.12A>G	NP_001363829.1:p.Glu4=
NM_020227.4:c.12A>G MANE Select	NP_064612.2:p.Glu4=