Canonical Allele Identifier: CA1921497506
Gene: POLR3A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.77980192C= , CM000672.2:g.77980192C= GRCh38
NC_000010.10:g.79739950C= , CM000672.1:g.79739950C= GRCh37
NC_000010.9:g.79409956C= NCBI36
NG_029648.1:g.54349G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000698724.1:n.1890G=
ENST00000698725.1:n.1643G=
ENST00000698726.1:n.3203G=
ENST00000698727.1:n.2936G=
ENST00000698728.1:n.3552G=
ENST00000698729.1:n.5000G=
ENST00000698730.1:n.5098G=
ENST00000698731.1:c.3832G= ENSP00000513898.1:p.Ala1278=
ENST00000698732.1:c.*2662G= ENSP00000513899.1:n.*2662G=
ENST00000698733.1:c.*3160G= ENSP00000513900.1:n.*3160G=
ENST00000698734.1:c.*2146G= ENSP00000513901.1:n.*2146G=
ENST00000698735.1:n.4324G=
ENST00000698736.1:n.4737G=
ENST00000698737.1:n.4088G=
ENST00000372371.8:c.3973G= MANE Select ENSP00000361446.3:p.Ala1325=
ENST00000372371.7:c.3973G= ENSP00000361446.3:p.Ala1325=
ENST00000616246.4:c.421G= ENSP00000483738.1:p.Ala141=
NM_007055.3:c.3973G= NP_008986.2:p.Ala1325=
NM_007055.4:c.3973G= MANE Select NP_008986.2:p.Ala1325=