Canonical Allele Identifier: CA1533058922

Gene: PRDM9

Linked Data

• dbSNP Id: rs1739034191

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.23508942_23508947dup , CM000667.2:g.23508942_23508947dup	GRCh38
NC_000005.9:g.23509051_23509056dup , CM000667.1:g.23509051_23509056dup	GRCh37
NC_000005.8:g.23544808_23544813dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502755.6:c.-84-8_-84-3dup	ENSP00000425471.2:n.-84-8_-84-3dup
ENST00000296682.4:c.-84-8_-84-3dup MANE Select	ENSP00000296682.4:n.-84-8_-84-3dup
ENST00000296682.3:c.-84-8_-84-3dup	ENSP00000296682.3:n.-84-8_-84-3dup
ENST00000502755.5:c.-84-8_-84-3dup	ENSP00000425471.1:n.-84-8_-84-3dup
ENST00000635252.1:c.17-978_17-973dup	ENSP00000489227.1:n.17-978_17-973dup
NM_020227.2:c.-84-8_-84-3dup	NP_064612.2:n.-84-8_-84-3dup
NM_020227.3:c.-84-8_-84-3dup	NP_064612.2:n.-84-8_-84-3dup
NM_001376900.1:c.-84-8_-84-3dup	NP_001363829.1:n.-84-8_-84-3dup
NM_020227.4:c.-84-8_-84-3dup MANE Select	NP_064612.2:n.-84-8_-84-3dup