Canonical Allele Identifier: CA1653274734

Gene: PRDM1 ATG5

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.106099422C= , CM000668.2:g.106099422C=	GRCh38
NC_000006.11:g.106547297C= , CM000668.1:g.106547297C=	GRCh37
NC_000006.10:g.106653990C=	NCBI36
NG_029115.1:g.18103C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369096.9:c.534C= (PRDM1) MANE Select	ENSP00000358092.4:p.Asn178=
ENST00000636335.1:c.458-21107G= (ATG5)	ENSP00000490221.1:n.458-21107G=
ENST00000636437.1:c.458-52597G= (ATG5)	ENSP00000490376.1:n.458-52597G=
ENST00000648754.1:c.576C= (PRDM1)	ENSP00000498029.1:p.Asn192=
ENST00000651185.1:c.426C= (PRDM1)	ENSP00000498716.1:p.Asn142=
ENST00000652320.1:c.426C= (PRDM1)	ENSP00000498580.1:p.Asn142=
ENST00000369089.3:c.132C= (PRDM1)	ENSP00000358085.3:p.Asn44=
ENST00000369091.6:c.426C= (PRDM1)	ENSP00000358087.2:p.Asn142=
ENST00000369096.8:c.534C= (PRDM1)	ENSP00000358092.4:p.Asn178=
ENST00000450060.5:c.171C= (PRDM1)	ENSP00000399772.1:p.Asn57=
ENST00000481163.1:n.293C= (PRDM1)
ENST00000613999.4:c.426C= (PRDM1)	ENSP00000478294.1:p.Asn142=
NM_001198.3:c.534C= (PRDM1)	NP_001189.2:p.Asn178=
NM_182907.2:c.132C= (PRDM1)	NP_878911.1:p.Asn44=
XM_005267094.3:c.60C= (PRDM1)	XP_005267151.1:p.Asn20=
XM_006715550.2:c.576C= (PRDM1)	XP_006715613.1:p.Asn192=
XM_011536062.1:c.576C= (PRDM1)	XP_011534364.1:p.Asn192=
XM_011536063.1:c.426C= (PRDM1)	XP_011534365.1:p.Asn142=
XM_011536064.1:c.60C= (PRDM1)	XP_011534366.1:p.Asn20=
XM_006715550.3:c.576C= (PRDM1)	XP_006715613.1:p.Asn192=
XM_011536062.3:c.576C= (PRDM1)	XP_011534364.1:p.Asn192=
XM_011536063.2:c.426C= (PRDM1)	XP_011534365.1:p.Asn142=
XM_011536064.3:c.60C= (PRDM1)	XP_011534366.1:p.Asn20=
XM_017011187.1:c.426C= (PRDM1)	XP_016866676.1:p.Asn142=
NM_001198.4:c.534C= (PRDM1) MANE Select	NP_001189.2:p.Asn178=
NM_182907.3:c.132C= (PRDM1)	NP_878911.1:p.Asn44=