Canonical Allele Identifier: CA359307504

Gene: PRDM9

Linked Data

• dbSNP Id: rs1739036731
• MyVariant Identifiers: chr5:g.23509150C>T (hg19) ; chr5:g.23509041C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.23509041C>T , CM000667.2:g.23509041C>T	GRCh38
NC_000005.9:g.23509150C>T , CM000667.1:g.23509150C>T	GRCh37
NC_000005.8:g.23544907C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502755.6:c.8C>T	ENSP00000425471.2:p.Pro3Leu
ENST00000296682.4:c.8C>T MANE Select	ENSP00000296682.4:p.Pro3Leu
ENST00000296682.3:c.8C>T	ENSP00000296682.3:p.Pro3Leu
ENST00000502755.5:c.8C>T	ENSP00000425471.1:p.Pro3Leu
ENST00000635252.1:c.17-879C>T	ENSP00000489227.1:n.17-879C>T
NM_020227.2:c.8C>T	NP_064612.2:p.Pro3Leu
NM_020227.3:c.8C>T	NP_064612.2:p.Pro3Leu
NM_001376900.1:c.8C>T	NP_001363829.1:p.Pro3Leu
NM_020227.4:c.8C>T MANE Select	NP_064612.2:p.Pro3Leu