Canonical Allele Identifier: CA443558081
Gene: PRDM9 HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.23509157G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.23509048G>A , CM000667.2:g.23509048G>A GRCh38
NC_000005.9:g.23509157G>A , CM000667.1:g.23509157G>A GRCh37
NC_000005.8:g.23544914G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000502755.6:c.15G>A ENSP00000425471.2:p.Lys5=
ENST00000296682.4:c.15G>A MANE Select ENSP00000296682.4:p.Lys5=
ENST00000296682.3:c.15G>A ENSP00000296682.3:p.Lys5=
ENST00000502755.5:c.15G>A ENSP00000425471.1:p.Lys5=
ENST00000635252.1:c.17-872G>A ENSP00000489227.1:n.17-872G>A
NM_020227.2:c.15G>A NP_064612.2:p.Lys5=
NM_020227.3:c.15G>A NP_064612.2:p.Lys5=
NM_001376900.1:c.15G>A NP_001363829.1:p.Lys5=
NM_020227.4:c.15G>A MANE Select NP_064612.2:p.Lys5=