Canonical Allele Identifier: CA365146776

Gene: PRDM1 ATG5

Linked Data

• MyVariant Identifiers: chr6:g.106547276A>C (hg19) ; chr6:g.106099401A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.106099401A>C , CM000668.2:g.106099401A>C	GRCh38
NC_000006.11:g.106547276A>C , CM000668.1:g.106547276A>C	GRCh37
NC_000006.10:g.106653969A>C	NCBI36
NG_029115.1:g.18082A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369096.9:c.513A>C (PRDM1) MANE Select	ENSP00000358092.4:p.Gln171His
ENST00000636335.1:c.458-21086T>G (ATG5)	ENSP00000490221.1:n.458-21086T>G
ENST00000636437.1:c.458-52576T>G (ATG5)	ENSP00000490376.1:n.458-52576T>G
ENST00000648754.1:c.555A>C (PRDM1)	ENSP00000498029.1:p.Gln185His
ENST00000651185.1:c.405A>C (PRDM1)	ENSP00000498716.1:p.Gln135His
ENST00000652320.1:c.405A>C (PRDM1)	ENSP00000498580.1:p.Gln135His
ENST00000369089.3:c.111A>C (PRDM1)	ENSP00000358085.3:p.Gln37His
ENST00000369091.6:c.405A>C (PRDM1)	ENSP00000358087.2:p.Gln135His
ENST00000369096.8:c.513A>C (PRDM1)	ENSP00000358092.4:p.Gln171His
ENST00000450060.5:c.150A>C (PRDM1)	ENSP00000399772.1:p.Gln50His
ENST00000481163.1:n.272A>C (PRDM1)
ENST00000613999.4:c.405A>C (PRDM1)	ENSP00000478294.1:p.Gln135His
NM_001198.3:c.513A>C (PRDM1)	NP_001189.2:p.Gln171His
NM_182907.2:c.111A>C (PRDM1)	NP_878911.1:p.Gln37His
XM_005267094.3:c.39A>C (PRDM1)	XP_005267151.1:p.Gln13His
XM_006715550.2:c.555A>C (PRDM1)	XP_006715613.1:p.Gln185His
XM_011536062.1:c.555A>C (PRDM1)	XP_011534364.1:p.Gln185His
XM_011536063.1:c.405A>C (PRDM1)	XP_011534365.1:p.Gln135His
XM_011536064.1:c.39A>C (PRDM1)	XP_011534366.1:p.Gln13His
XM_006715550.3:c.555A>C (PRDM1)	XP_006715613.1:p.Gln185His
XM_011536062.3:c.555A>C (PRDM1)	XP_011534364.1:p.Gln185His
XM_011536063.2:c.405A>C (PRDM1)	XP_011534365.1:p.Gln135His
XM_011536064.3:c.39A>C (PRDM1)	XP_011534366.1:p.Gln13His
XM_017011187.1:c.405A>C (PRDM1)	XP_016866676.1:p.Gln135His
NM_001198.4:c.513A>C (PRDM1) MANE Select	NP_001189.2:p.Gln171His
NM_182907.3:c.111A>C (PRDM1)	NP_878911.1:p.Gln37His