Canonical Allele Identifier: CA2788643994
Gene: POLR3A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.78009786_78009791del , CM000672.2:g.78009786_78009791del GRCh38
NC_000010.10:g.79769544_79769549del , CM000672.1:g.79769544_79769549del GRCh37
NC_000010.9:g.79439550_79439555del NCBI36
NG_029648.1:g.24751_24756del

Transcript Alleles

HGVS Amino-acid Change
ENST00000698728.1:n.1349+74_1349+79del
ENST00000698729.1:n.2895+74_2895+79del
ENST00000698730.1:n.2895+74_2895+79del
ENST00000698731.1:c.1629+74_1629+79del ENSP00000513898.1:n.1629+74_1629+79del
ENST00000698732.1:c.*631+74_*631+79del ENSP00000513899.1:n.*631+74_*631+79del
ENST00000698733.1:c.*957+74_*957+79del ENSP00000513900.1:n.*957+74_*957+79del
ENST00000698734.1:c.1770+74_1770+79del ENSP00000513901.1:n.1770+74_1770+79del
ENST00000698735.1:n.1885+74_1885+79del
ENST00000698736.1:n.1885+74_1885+79del
ENST00000698737.1:n.1885+74_1885+79del
ENST00000698738.1:n.1885+74_1885+79del
ENST00000698739.1:n.1885+74_1885+79del
ENST00000372371.8:c.1770+74_1770+79del MANE Select ENSP00000361446.3:n.1770+74_1770+79del
ENST00000372371.7:c.1770+74_1770+79del ENSP00000361446.3:n.1770+74_1770+79del
ENST00000473588.2:c.572+74_572+79del
NM_007055.3:c.1770+74_1770+79del NP_008986.2:n.1770+74_1770+79del
NM_007055.4:c.1770+74_1770+79del MANE Select NP_008986.2:n.1770+74_1770+79del