Canonical Allele Identifier: CA365146798

Gene: PRDM1 ATG5

Linked Data

• MyVariant Identifiers: chr6:g.106547286G>C (hg19) ; chr6:g.106099411G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.106099411G>C , CM000668.2:g.106099411G>C	GRCh38
NC_000006.11:g.106547286G>C , CM000668.1:g.106547286G>C	GRCh37
NC_000006.10:g.106653979G>C	NCBI36
NG_029115.1:g.18092G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369096.9:c.523G>C (PRDM1) MANE Select	ENSP00000358092.4:p.Ala175Pro
ENST00000636335.1:c.458-21096C>G (ATG5)	ENSP00000490221.1:n.458-21096C>G
ENST00000636437.1:c.458-52586C>G (ATG5)	ENSP00000490376.1:n.458-52586C>G
ENST00000648754.1:c.565G>C (PRDM1)	ENSP00000498029.1:p.Ala189Pro
ENST00000651185.1:c.415G>C (PRDM1)	ENSP00000498716.1:p.Ala139Pro
ENST00000652320.1:c.415G>C (PRDM1)	ENSP00000498580.1:p.Ala139Pro
ENST00000369089.3:c.121G>C (PRDM1)	ENSP00000358085.3:p.Ala41Pro
ENST00000369091.6:c.415G>C (PRDM1)	ENSP00000358087.2:p.Ala139Pro
ENST00000369096.8:c.523G>C (PRDM1)	ENSP00000358092.4:p.Ala175Pro
ENST00000450060.5:c.160G>C (PRDM1)	ENSP00000399772.1:p.Ala54Pro
ENST00000481163.1:n.282G>C (PRDM1)
ENST00000613999.4:c.415G>C (PRDM1)	ENSP00000478294.1:p.Ala139Pro
NM_001198.3:c.523G>C (PRDM1)	NP_001189.2:p.Ala175Pro
NM_182907.2:c.121G>C (PRDM1)	NP_878911.1:p.Ala41Pro
XM_005267094.3:c.49G>C (PRDM1)	XP_005267151.1:p.Ala17Pro
XM_006715550.2:c.565G>C (PRDM1)	XP_006715613.1:p.Ala189Pro
XM_011536062.1:c.565G>C (PRDM1)	XP_011534364.1:p.Ala189Pro
XM_011536063.1:c.415G>C (PRDM1)	XP_011534365.1:p.Ala139Pro
XM_011536064.1:c.49G>C (PRDM1)	XP_011534366.1:p.Ala17Pro
XM_006715550.3:c.565G>C (PRDM1)	XP_006715613.1:p.Ala189Pro
XM_011536062.3:c.565G>C (PRDM1)	XP_011534364.1:p.Ala189Pro
XM_011536063.2:c.415G>C (PRDM1)	XP_011534365.1:p.Ala139Pro
XM_011536064.3:c.49G>C (PRDM1)	XP_011534366.1:p.Ala17Pro
XM_017011187.1:c.415G>C (PRDM1)	XP_016866676.1:p.Ala139Pro
NM_001198.4:c.523G>C (PRDM1) MANE Select	NP_001189.2:p.Ala175Pro
NM_182907.3:c.121G>C (PRDM1)	NP_878911.1:p.Ala41Pro