Canonical Allele Identifier: CA365146814

Linked Data

dbSNP Id: rs1472659431

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.106099418A>C , CM000668.2:g.106099418A>C GRCh38
NC_000006.11:g.106547293A>C , CM000668.1:g.106547293A>C GRCh37
NC_000006.10:g.106653986A>C NCBI36
NG_029115.1:g.18099A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000369096.9:c.530A>C (PRDM1) MANE Select ENSP00000358092.4:p.Gln177Pro
ENST00000636335.1:c.458-21103T>G (ATG5) ENSP00000490221.1:n.458-21103T>G
ENST00000636437.1:c.458-52593T>G (ATG5) ENSP00000490376.1:n.458-52593T>G
ENST00000648754.1:c.572A>C (PRDM1) ENSP00000498029.1:p.Gln191Pro
ENST00000651185.1:c.422A>C (PRDM1) ENSP00000498716.1:p.Gln141Pro
ENST00000652320.1:c.422A>C (PRDM1) ENSP00000498580.1:p.Gln141Pro
ENST00000369089.3:c.128A>C (PRDM1) ENSP00000358085.3:p.Gln43Pro
ENST00000369091.6:c.422A>C (PRDM1) ENSP00000358087.2:p.Gln141Pro
ENST00000369096.8:c.530A>C (PRDM1) ENSP00000358092.4:p.Gln177Pro
ENST00000450060.5:c.167A>C (PRDM1) ENSP00000399772.1:p.Gln56Pro
ENST00000481163.1:n.289A>C (PRDM1)
ENST00000613999.4:c.422A>C (PRDM1) ENSP00000478294.1:p.Gln141Pro
NM_001198.3:c.530A>C (PRDM1) NP_001189.2:p.Gln177Pro
NM_182907.2:c.128A>C (PRDM1) NP_878911.1:p.Gln43Pro
XM_005267094.3:c.56A>C (PRDM1) XP_005267151.1:p.Gln19Pro
XM_006715550.2:c.572A>C (PRDM1) XP_006715613.1:p.Gln191Pro
XM_011536062.1:c.572A>C (PRDM1) XP_011534364.1:p.Gln191Pro
XM_011536063.1:c.422A>C (PRDM1) XP_011534365.1:p.Gln141Pro
XM_011536064.1:c.56A>C (PRDM1) XP_011534366.1:p.Gln19Pro
XM_006715550.3:c.572A>C (PRDM1) XP_006715613.1:p.Gln191Pro
XM_011536062.3:c.572A>C (PRDM1) XP_011534364.1:p.Gln191Pro
XM_011536063.2:c.422A>C (PRDM1) XP_011534365.1:p.Gln141Pro
XM_011536064.3:c.56A>C (PRDM1) XP_011534366.1:p.Gln19Pro
XM_017011187.1:c.422A>C (PRDM1) XP_016866676.1:p.Gln141Pro
NM_001198.4:c.530A>C (PRDM1) MANE Select NP_001189.2:p.Gln177Pro
NM_182907.3:c.128A>C (PRDM1) NP_878911.1:p.Gln43Pro