Canonical Allele Identifier: CA359307514
Gene: PRDM9 HGNC NCBI

Linked Data

dbSNP Id: rs1739036894
COSMIC: COSM4408067
MyVariant Identifiers: chr5:g.23509156A>C (hg19) chr5:g.23509047A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.23509047A>C , CM000667.2:g.23509047A>C GRCh38
NC_000005.9:g.23509156A>C , CM000667.1:g.23509156A>C GRCh37
NC_000005.8:g.23544913A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000502755.6:c.14A>C ENSP00000425471.2:p.Lys5Thr
ENST00000296682.4:c.14A>C MANE Select ENSP00000296682.4:p.Lys5Thr
ENST00000296682.3:c.14A>C ENSP00000296682.3:p.Lys5Thr
ENST00000502755.5:c.14A>C ENSP00000425471.1:p.Lys5Thr
ENST00000635252.1:c.17-873A>C ENSP00000489227.1:n.17-873A>C
NM_020227.2:c.14A>C NP_064612.2:p.Lys5Thr
NM_020227.3:c.14A>C NP_064612.2:p.Lys5Thr
NM_001376900.1:c.14A>C NP_001363829.1:p.Lys5Thr
NM_020227.4:c.14A>C MANE Select NP_064612.2:p.Lys5Thr
Search 100 bp 5'
Search 100 bp 3'