Canonical Allele Identifier: CA2317513028
Gene: POLR2E HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1093981C= , CM000681.2:g.1093981C= GRCh38
NC_000019.9:g.1093980C= , CM000681.1:g.1093980C= GRCh37
NC_000019.8:g.1044980C= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000615234.5:c.155G= MANE Select ENSP00000478303.1:p.Arg52=
ENST00000215587.11:c.155G= ENSP00000215587.7:p.Arg52=
ENST00000585838.2:c.3+1278G=
ENST00000586746.5:c.155G= ENSP00000464739.1:p.Arg52=
ENST00000586817.5:n.1395G=
ENST00000589737.5:c.57+1278G= ENSP00000467905.1:n.57+1278G=
ENST00000591709.1:n.201G=
ENST00000591767.5:c.58-78G= ENSP00000465066.1:n.58-78G=
ENST00000592597.1:n.189G=
ENST00000612655.4:c.155G= ENSP00000485021.1:p.Arg52=
ENST00000614705.4:n.194G=
ENST00000615234.4:c.155G= ENSP00000478303.1:p.Arg52=
ENST00000619917.4:c.155G= ENSP00000479813.1:p.Arg52=
NM_001316323.1:c.-48+1278G= NP_001303252.1:n.-48+1278G=
NM_001316324.1:c.-195-78G= NP_001303253.1:n.-195-78G=
NM_002695.3:c.155G= NP_002686.2:p.Arg52=
XM_011528070.1:c.155G= XP_011526372.1:p.Arg52=
XM_011528070.3:c.155G= XP_011526372.1:p.Arg52=
XM_017026883.2:c.-48+1278G= XP_016882372.1:n.-48+1278G=
NM_002695.4:c.155G= NP_002686.2:p.Arg52=
NM_001316323.2:c.-48+1278G= NP_001303252.1:n.-48+1278G=
NM_001316324.2:c.-195-78G= NP_001303253.1:n.-195-78G=
NM_002695.5:c.155G= MANE Select NP_002686.3:p.Arg52=