Canonical Allele Identifier: CA365146738

Gene: PRDM1 ATG5

Linked Data

• dbSNP Id: rs769455910
• MyVariant Identifiers: chr6:g.106547256G>A (hg19) ; chr6:g.106099381G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.106099381G>A , CM000668.2:g.106099381G>A	GRCh38
NC_000006.11:g.106547256G>A , CM000668.1:g.106547256G>A	GRCh37
NC_000006.10:g.106653949G>A	NCBI36
NG_029115.1:g.18062G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369096.9:c.493G>A (PRDM1) MANE Select	ENSP00000358092.4:p.Ala165Thr
ENST00000636335.1:c.458-21066C>T (ATG5)	ENSP00000490221.1:n.458-21066C>T
ENST00000636437.1:c.458-52556C>T (ATG5)	ENSP00000490376.1:n.458-52556C>T
ENST00000648754.1:c.535G>A (PRDM1)	ENSP00000498029.1:p.Ala179Thr
ENST00000651185.1:c.385G>A (PRDM1)	ENSP00000498716.1:p.Ala129Thr
ENST00000652320.1:c.385G>A (PRDM1)	ENSP00000498580.1:p.Ala129Thr
ENST00000369089.3:c.91G>A (PRDM1)	ENSP00000358085.3:p.Ala31Thr
ENST00000369091.6:c.385G>A (PRDM1)	ENSP00000358087.2:p.Ala129Thr
ENST00000369096.8:c.493G>A (PRDM1)	ENSP00000358092.4:p.Ala165Thr
ENST00000450060.5:c.130G>A (PRDM1)	ENSP00000399772.1:p.Ala44Thr
ENST00000481163.1:n.252G>A (PRDM1)
ENST00000613999.4:c.385G>A (PRDM1)	ENSP00000478294.1:p.Ala129Thr
NM_001198.3:c.493G>A (PRDM1)	NP_001189.2:p.Ala165Thr
NM_182907.2:c.91G>A (PRDM1)	NP_878911.1:p.Ala31Thr
XM_005267094.3:c.19G>A (PRDM1)	XP_005267151.1:p.Ala7Thr
XM_006715550.2:c.535G>A (PRDM1)	XP_006715613.1:p.Ala179Thr
XM_011536062.1:c.535G>A (PRDM1)	XP_011534364.1:p.Ala179Thr
XM_011536063.1:c.385G>A (PRDM1)	XP_011534365.1:p.Ala129Thr
XM_011536064.1:c.19G>A (PRDM1)	XP_011534366.1:p.Ala7Thr
XM_006715550.3:c.535G>A (PRDM1)	XP_006715613.1:p.Ala179Thr
XM_011536062.3:c.535G>A (PRDM1)	XP_011534364.1:p.Ala179Thr
XM_011536063.2:c.385G>A (PRDM1)	XP_011534365.1:p.Ala129Thr
XM_011536064.3:c.19G>A (PRDM1)	XP_011534366.1:p.Ala7Thr
XM_017011187.1:c.385G>A (PRDM1)	XP_016866676.1:p.Ala129Thr
NM_001198.4:c.493G>A (PRDM1) MANE Select	NP_001189.2:p.Ala165Thr
NM_182907.3:c.91G>A (PRDM1)	NP_878911.1:p.Ala31Thr