Canonical Allele Identifier: CA668635766
Gene: POLR3A HGNC NCBI

Linked Data

dbSNP Id: rs1305093676

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.77980362del , CM000672.2:g.77980362del GRCh38
NC_000010.10:g.79740120del , CM000672.1:g.79740120del GRCh37
NC_000010.9:g.79410126del NCBI36
NG_029648.1:g.54179del

Transcript Alleles

HGVS Amino-acid Change
ENST00000698724.1:n.1809-89del
ENST00000698725.1:n.1473del
ENST00000698726.1:n.3122-89del
ENST00000698727.1:n.2855-89del
ENST00000698728.1:n.3471-89del
ENST00000698729.1:n.4919-89del
ENST00000698730.1:n.5017-89del
ENST00000698731.1:c.3751-89del ENSP00000513898.1:n.3751-89del
ENST00000698732.1:c.*2581-89del ENSP00000513899.1:n.*2581-89del
ENST00000698733.1:c.*3079-89del ENSP00000513900.1:n.*3079-89del
ENST00000698734.1:c.*2065-89del ENSP00000513901.1:n.*2065-89del
ENST00000698735.1:n.4243-89del
ENST00000698736.1:n.4656-89del
ENST00000698737.1:n.4007-89del
ENST00000372371.8:c.3892-89del MANE Select ENSP00000361446.3:n.3892-89del
ENST00000372371.7:c.3892-89del ENSP00000361446.3:n.3892-89del
ENST00000616246.4:c.340-89del ENSP00000483738.1:n.340-89del
NM_007055.3:c.3892-89del NP_008986.2:n.3892-89del
NM_007055.4:c.3892-89del MANE Select NP_008986.2:n.3892-89del