Canonical Allele Identifier: CA1921497578
Gene: POLR3A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.77980349T= , CM000672.2:g.77980349T= GRCh38
NC_000010.10:g.79740107T= , CM000672.1:g.79740107T= GRCh37
NC_000010.9:g.79410113T= NCBI36
NG_029648.1:g.54192A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000698724.1:n.1809-76A=
ENST00000698725.1:n.1486A=
ENST00000698726.1:n.3122-76A=
ENST00000698727.1:n.2855-76A=
ENST00000698728.1:n.3471-76A=
ENST00000698729.1:n.4919-76A=
ENST00000698730.1:n.5017-76A=
ENST00000698731.1:c.3751-76A= ENSP00000513898.1:n.3751-76A=
ENST00000698732.1:c.*2581-76A= ENSP00000513899.1:n.*2581-76A=
ENST00000698733.1:c.*3079-76A= ENSP00000513900.1:n.*3079-76A=
ENST00000698734.1:c.*2065-76A= ENSP00000513901.1:n.*2065-76A=
ENST00000698735.1:n.4243-76A=
ENST00000698736.1:n.4656-76A=
ENST00000698737.1:n.4007-76A=
ENST00000372371.8:c.3892-76A= MANE Select ENSP00000361446.3:n.3892-76A=
ENST00000372371.7:c.3892-76A= ENSP00000361446.3:n.3892-76A=
ENST00000616246.4:c.340-76A= ENSP00000483738.1:n.340-76A=
NM_007055.3:c.3892-76A= NP_008986.2:n.3892-76A=
NM_007055.4:c.3892-76A= MANE Select NP_008986.2:n.3892-76A=