Canonical Allele Identifier: CA1653274639

Gene: PRDM1 ATG5

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.106099346A= , CM000668.2:g.106099346A=	GRCh38
NC_000006.11:g.106547221A= , CM000668.1:g.106547221A=	GRCh37
NC_000006.10:g.106653914A=	NCBI36
NG_029115.1:g.18027A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369096.9:c.458A= (PRDM1) MANE Select	ENSP00000358092.4:p.Glu153=
ENST00000636335.1:c.458-21031T= (ATG5)	ENSP00000490221.1:n.458-21031T=
ENST00000636437.1:c.458-52521T= (ATG5)	ENSP00000490376.1:n.458-52521T=
ENST00000648754.1:c.500A= (PRDM1)	ENSP00000498029.1:p.Glu167=
ENST00000651185.1:c.350A= (PRDM1)	ENSP00000498716.1:p.Glu117=
ENST00000652320.1:c.350A= (PRDM1)	ENSP00000498580.1:p.Glu117=
ENST00000369089.3:c.56A= (PRDM1)	ENSP00000358085.3:p.Glu19=
ENST00000369091.6:c.350A= (PRDM1)	ENSP00000358087.2:p.Glu117=
ENST00000369096.8:c.458A= (PRDM1)	ENSP00000358092.4:p.Glu153=
ENST00000450060.5:c.95A= (PRDM1)	ENSP00000399772.1:p.Glu32=
ENST00000481163.1:n.217A= (PRDM1)
ENST00000613999.4:c.350A= (PRDM1)	ENSP00000478294.1:p.Glu117=
NM_001198.3:c.458A= (PRDM1)	NP_001189.2:p.Glu153=
NM_182907.2:c.56A= (PRDM1)	NP_878911.1:p.Glu19=
XM_005267094.3:c.-17A= (PRDM1)	XP_005267151.1:n.-17A=
XM_006715550.2:c.500A= (PRDM1)	XP_006715613.1:p.Glu167=
XM_011536062.1:c.500A= (PRDM1)	XP_011534364.1:p.Glu167=
XM_011536063.1:c.350A= (PRDM1)	XP_011534365.1:p.Glu117=
XM_011536064.1:c.-17A= (PRDM1)	XP_011534366.1:n.-17A=
XM_006715550.3:c.500A= (PRDM1)	XP_006715613.1:p.Glu167=
XM_011536062.3:c.500A= (PRDM1)	XP_011534364.1:p.Glu167=
XM_011536063.2:c.350A= (PRDM1)	XP_011534365.1:p.Glu117=
XM_011536064.3:c.-17A= (PRDM1)	XP_011534366.1:n.-17A=
XM_017011187.1:c.350A= (PRDM1)	XP_016866676.1:p.Glu117=
NM_001198.4:c.458A= (PRDM1) MANE Select	NP_001189.2:p.Glu153=
NM_182907.3:c.56A= (PRDM1)	NP_878911.1:p.Glu19=