Canonical Allele Identifier: CA1533058934

Gene: PRDM9

Linked Data

• dbSNP Id: rs1739034500

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.23508968_23508974del , CM000667.2:g.23508968_23508974del	GRCh38
NC_000005.9:g.23509077_23509083del , CM000667.1:g.23509077_23509083del	GRCh37
NC_000005.8:g.23544834_23544840del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502755.6:c.-66_-60del	ENSP00000425471.2:n.-66_-60del
ENST00000296682.4:c.-66_-60del MANE Select	ENSP00000296682.4:n.-66_-60del
ENST00000296682.3:c.-66_-60del	ENSP00000296682.3:n.-66_-60del
ENST00000502755.5:c.-66_-60del	ENSP00000425471.1:n.-66_-60del
ENST00000635252.1:c.17-952_17-946del	ENSP00000489227.1:n.17-952_17-946del
NM_020227.2:c.-66_-60del	NP_064612.2:n.-66_-60del
NM_020227.3:c.-66_-60del	NP_064612.2:n.-66_-60del
NM_001376900.1:c.-66_-60del	NP_001363829.1:n.-66_-60del
NM_020227.4:c.-66_-60del MANE Select	NP_064612.2:n.-66_-60del