Canonical Allele Identifier: CA365146787

Gene: PRDM1 ATG5

Linked Data

• dbSNP Id: rs2114638480
• MyVariant Identifiers: chr6:g.106547280C>G (hg19) ; chr6:g.106099405C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.106099405C>G , CM000668.2:g.106099405C>G	GRCh38
NC_000006.11:g.106547280C>G , CM000668.1:g.106547280C>G	GRCh37
NC_000006.10:g.106653973C>G	NCBI36
NG_029115.1:g.18086C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369096.9:c.517C>G (PRDM1) MANE Select	ENSP00000358092.4:p.Leu173Val
ENST00000636335.1:c.458-21090G>C (ATG5)	ENSP00000490221.1:n.458-21090G>C
ENST00000636437.1:c.458-52580G>C (ATG5)	ENSP00000490376.1:n.458-52580G>C
ENST00000648754.1:c.559C>G (PRDM1)	ENSP00000498029.1:p.Leu187Val
ENST00000651185.1:c.409C>G (PRDM1)	ENSP00000498716.1:p.Leu137Val
ENST00000652320.1:c.409C>G (PRDM1)	ENSP00000498580.1:p.Leu137Val
ENST00000369089.3:c.115C>G (PRDM1)	ENSP00000358085.3:p.Leu39Val
ENST00000369091.6:c.409C>G (PRDM1)	ENSP00000358087.2:p.Leu137Val
ENST00000369096.8:c.517C>G (PRDM1)	ENSP00000358092.4:p.Leu173Val
ENST00000450060.5:c.154C>G (PRDM1)	ENSP00000399772.1:p.Leu52Val
ENST00000481163.1:n.276C>G (PRDM1)
ENST00000613999.4:c.409C>G (PRDM1)	ENSP00000478294.1:p.Leu137Val
NM_001198.3:c.517C>G (PRDM1)	NP_001189.2:p.Leu173Val
NM_182907.2:c.115C>G (PRDM1)	NP_878911.1:p.Leu39Val
XM_005267094.3:c.43C>G (PRDM1)	XP_005267151.1:p.Leu15Val
XM_006715550.2:c.559C>G (PRDM1)	XP_006715613.1:p.Leu187Val
XM_011536062.1:c.559C>G (PRDM1)	XP_011534364.1:p.Leu187Val
XM_011536063.1:c.409C>G (PRDM1)	XP_011534365.1:p.Leu137Val
XM_011536064.1:c.43C>G (PRDM1)	XP_011534366.1:p.Leu15Val
XM_006715550.3:c.559C>G (PRDM1)	XP_006715613.1:p.Leu187Val
XM_011536062.3:c.559C>G (PRDM1)	XP_011534364.1:p.Leu187Val
XM_011536063.2:c.409C>G (PRDM1)	XP_011534365.1:p.Leu137Val
XM_011536064.3:c.43C>G (PRDM1)	XP_011534366.1:p.Leu15Val
XM_017011187.1:c.409C>G (PRDM1)	XP_016866676.1:p.Leu137Val
NM_001198.4:c.517C>G (PRDM1) MANE Select	NP_001189.2:p.Leu173Val
NM_182907.3:c.115C>G (PRDM1)	NP_878911.1:p.Leu39Val