Canonical Allele Identifier: CA2673377931

Gene: PRDM9

Linked Data

• gnomAD v4: 5-23508970-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.23508970G>T , CM000667.2:g.23508970G>T	GRCh38
NC_000005.9:g.23509079G>T , CM000667.1:g.23509079G>T	GRCh37
NC_000005.8:g.23544836G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000502755.6:c.-64G>T	ENSP00000425471.2:n.-64G>T
ENST00000296682.4:c.-64G>T MANE Select	ENSP00000296682.4:n.-64G>T
ENST00000296682.3:c.-64G>T	ENSP00000296682.3:n.-64G>T
ENST00000502755.5:c.-64G>T	ENSP00000425471.1:n.-64G>T
ENST00000635252.1:c.17-950G>T	ENSP00000489227.1:n.17-950G>T
NM_020227.2:c.-64G>T	NP_064612.2:n.-64G>T
NM_020227.3:c.-64G>T	NP_064612.2:n.-64G>T
NM_001376900.1:c.-64G>T	NP_001363829.1:n.-64G>T
NM_020227.4:c.-64G>T MANE Select	NP_064612.2:n.-64G>T