Canonical Allele Identifier: CA443558039
Gene: PRDM9 HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.23509151T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.23509042T>C , CM000667.2:g.23509042T>C GRCh38
NC_000005.9:g.23509151T>C , CM000667.1:g.23509151T>C GRCh37
NC_000005.8:g.23544908T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000502755.6:c.9T>C ENSP00000425471.2:p.Pro3=
ENST00000296682.4:c.9T>C MANE Select ENSP00000296682.4:p.Pro3=
ENST00000296682.3:c.9T>C ENSP00000296682.3:p.Pro3=
ENST00000502755.5:c.9T>C ENSP00000425471.1:p.Pro3=
ENST00000635252.1:c.17-878T>C ENSP00000489227.1:n.17-878T>C
NM_020227.2:c.9T>C NP_064612.2:p.Pro3=
NM_020227.3:c.9T>C NP_064612.2:p.Pro3=
NM_001376900.1:c.9T>C NP_001363829.1:p.Pro3=
NM_020227.4:c.9T>C MANE Select NP_064612.2:p.Pro3=