Canonical Allele Identifier: CA1533058933

Gene: PRDM9

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.23508963_23508970delinsAGGAGCTG , CM000667.2:g.23508963_23508970delinsAGGAGCTG	GRCh38
NC_000005.9:g.23509072_23509079delinsAGGAGCTG , CM000667.1:g.23509072_23509079delinsAGGAGCTG	GRCh37
NC_000005.8:g.23544829_23544836delinsAGGAGCTG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502755.6:c.-71_-64delinsAGGAGCTG	ENSP00000425471.2:n.-71_-64delinsAGGAGCTG
ENST00000296682.4:c.-71_-64delinsAGGAGCTG MANE Select	ENSP00000296682.4:n.-71_-64delinsAGGAGCTG
ENST00000296682.3:c.-71_-64delinsAGGAGCTG	ENSP00000296682.3:n.-71_-64delinsAGGAGCTG
ENST00000502755.5:c.-71_-64delinsAGGAGCTG	ENSP00000425471.1:n.-71_-64delinsAGGAGCTG
ENST00000635252.1:c.17-957_17-950delinsAGGAGCTG	ENSP00000489227.1:n.17-957_17-950delinsAGGAGCTG
NM_020227.2:c.-71_-64delinsAGGAGCTG	NP_064612.2:n.-71_-64delinsAGGAGCTG
NM_020227.3:c.-71_-64delinsAGGAGCTG	NP_064612.2:n.-71_-64delinsAGGAGCTG
NM_001376900.1:c.-71_-64delinsAGGAGCTG	NP_001363829.1:n.-71_-64delinsAGGAGCTG
NM_020227.4:c.-71_-64delinsAGGAGCTG MANE Select	NP_064612.2:n.-71_-64delinsAGGAGCTG