Canonical Allele Identifier: CA1921497514
Gene: POLR3A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.77980217C= , CM000672.2:g.77980217C= GRCh38
NC_000010.10:g.79739975C= , CM000672.1:g.79739975C= GRCh37
NC_000010.9:g.79409981C= NCBI36
NG_029648.1:g.54324G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000698724.1:n.1865G=
ENST00000698725.1:n.1618G=
ENST00000698726.1:n.3178G=
ENST00000698727.1:n.2911G=
ENST00000698728.1:n.3527G=
ENST00000698729.1:n.4975G=
ENST00000698730.1:n.5073G=
ENST00000698731.1:c.3807G= ENSP00000513898.1:p.Leu1269=
ENST00000698732.1:c.*2637G= ENSP00000513899.1:n.*2637G=
ENST00000698733.1:c.*3135G= ENSP00000513900.1:n.*3135G=
ENST00000698734.1:c.*2121G= ENSP00000513901.1:n.*2121G=
ENST00000698735.1:n.4299G=
ENST00000698736.1:n.4712G=
ENST00000698737.1:n.4063G=
ENST00000372371.8:c.3948G= MANE Select ENSP00000361446.3:p.Leu1316=
ENST00000372371.7:c.3948G= ENSP00000361446.3:p.Leu1316=
ENST00000616246.4:c.396G= ENSP00000483738.1:p.Leu132=
NM_007055.3:c.3948G= NP_008986.2:p.Leu1316=
NM_007055.4:c.3948G= MANE Select NP_008986.2:p.Leu1316=