Canonical Allele Identifier: CA2609821306
Gene: POLR3A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.77980388G>T , CM000672.2:g.77980388G>T GRCh38
NC_000010.10:g.79740146G>T , CM000672.1:g.79740146G>T GRCh37
NC_000010.9:g.79410152G>T NCBI36
NG_029648.1:g.54153C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000698724.1:n.1809-115C>A
ENST00000698725.1:n.1447C>A
ENST00000698726.1:n.3122-115C>A
ENST00000698727.1:n.2855-115C>A
ENST00000698728.1:n.3471-115C>A
ENST00000698729.1:n.4919-115C>A
ENST00000698730.1:n.5017-115C>A
ENST00000698731.1:c.3751-115C>A ENSP00000513898.1:n.3751-115C>A
ENST00000698732.1:c.*2581-115C>A ENSP00000513899.1:n.*2581-115C>A
ENST00000698733.1:c.*3079-115C>A ENSP00000513900.1:n.*3079-115C>A
ENST00000698734.1:c.*2065-115C>A ENSP00000513901.1:n.*2065-115C>A
ENST00000698735.1:n.4243-115C>A
ENST00000698736.1:n.4656-115C>A
ENST00000698737.1:n.4007-115C>A
ENST00000372371.8:c.3892-115C>A MANE Select ENSP00000361446.3:n.3892-115C>A
ENST00000372371.7:c.3892-115C>A ENSP00000361446.3:n.3892-115C>A
ENST00000616246.4:c.340-115C>A ENSP00000483738.1:n.340-115C>A
NM_007055.3:c.3892-115C>A NP_008986.2:n.3892-115C>A
NM_007055.4:c.3892-115C>A MANE Select NP_008986.2:n.3892-115C>A