Canonical Allele Identifier: CA210188880
Gene: POLR3A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.77982508A>C , CM000672.2:g.77982508A>C GRCh38
NC_000010.10:g.79742266A>C , CM000672.1:g.79742266A>C GRCh37
NC_000010.9:g.79412272A>C NCBI36
NG_029648.1:g.52033T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000698724.1:n.1511+145T>G
ENST00000698726.1:n.2824+145T>G
ENST00000698727.1:n.2557+145T>G
ENST00000698728.1:n.3173+145T>G
ENST00000698729.1:n.4621+145T>G
ENST00000698730.1:n.4719+145T>G
ENST00000698731.1:c.3453+145T>G ENSP00000513898.1:n.3453+145T>G
ENST00000698732.1:c.*2357+145T>G ENSP00000513899.1:n.*2357+145T>G
ENST00000698733.1:c.*2781+145T>G ENSP00000513900.1:n.*2781+145T>G
ENST00000698734.1:c.*1767+145T>G ENSP00000513901.1:n.*1767+145T>G
ENST00000698735.1:n.3756T>G
ENST00000698736.1:n.4358+145T>G
ENST00000698737.1:n.3709+145T>G
ENST00000372371.8:c.3594+145T>G MANE Select ENSP00000361446.3:n.3594+145T>G
ENST00000372371.7:c.3594+145T>G ENSP00000361446.3:n.3594+145T>G
ENST00000616246.4:c.42+145T>G ENSP00000483738.1:n.42+145T>G
NM_007055.3:c.3594+145T>G NP_008986.2:n.3594+145T>G
NM_007055.4:c.3594+145T>G MANE Select NP_008986.2:n.3594+145T>G