Canonical Allele Identifier: CA451576369

Linked Data

MyVariant Identifiers: chr6:g.106547267C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.106099392C>T , CM000668.2:g.106099392C>T GRCh38
NC_000006.11:g.106547267C>T , CM000668.1:g.106547267C>T GRCh37
NC_000006.10:g.106653960C>T NCBI36
NG_029115.1:g.18073C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000369096.9:c.504C>T (PRDM1) MANE Select ENSP00000358092.4:p.Pro168=
ENST00000636335.1:c.458-21077G>A (ATG5) ENSP00000490221.1:n.458-21077G>A
ENST00000636437.1:c.458-52567G>A (ATG5) ENSP00000490376.1:n.458-52567G>A
ENST00000648754.1:c.546C>T (PRDM1) ENSP00000498029.1:p.Pro182=
ENST00000651185.1:c.396C>T (PRDM1) ENSP00000498716.1:p.Pro132=
ENST00000652320.1:c.396C>T (PRDM1) ENSP00000498580.1:p.Pro132=
ENST00000369089.3:c.102C>T (PRDM1) ENSP00000358085.3:p.Pro34=
ENST00000369091.6:c.396C>T (PRDM1) ENSP00000358087.2:p.Pro132=
ENST00000369096.8:c.504C>T (PRDM1) ENSP00000358092.4:p.Pro168=
ENST00000450060.5:c.141C>T (PRDM1) ENSP00000399772.1:p.Pro47=
ENST00000481163.1:n.263C>T (PRDM1)
ENST00000613999.4:c.396C>T (PRDM1) ENSP00000478294.1:p.Pro132=
NM_001198.3:c.504C>T (PRDM1) NP_001189.2:p.Pro168=
NM_182907.2:c.102C>T (PRDM1) NP_878911.1:p.Pro34=
XM_005267094.3:c.30C>T (PRDM1) XP_005267151.1:p.Pro10=
XM_006715550.2:c.546C>T (PRDM1) XP_006715613.1:p.Pro182=
XM_011536062.1:c.546C>T (PRDM1) XP_011534364.1:p.Pro182=
XM_011536063.1:c.396C>T (PRDM1) XP_011534365.1:p.Pro132=
XM_011536064.1:c.30C>T (PRDM1) XP_011534366.1:p.Pro10=
XM_006715550.3:c.546C>T (PRDM1) XP_006715613.1:p.Pro182=
XM_011536062.3:c.546C>T (PRDM1) XP_011534364.1:p.Pro182=
XM_011536063.2:c.396C>T (PRDM1) XP_011534365.1:p.Pro132=
XM_011536064.3:c.30C>T (PRDM1) XP_011534366.1:p.Pro10=
XM_017011187.1:c.396C>T (PRDM1) XP_016866676.1:p.Pro132=
NM_001198.4:c.504C>T (PRDM1) MANE Select NP_001189.2:p.Pro168=
NM_182907.3:c.102C>T (PRDM1) NP_878911.1:p.Pro34=