Canonical Allele Identifier: CA1921497508
Gene: POLR3A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.77980194G= , CM000672.2:g.77980194G= GRCh38
NC_000010.10:g.79739952G= , CM000672.1:g.79739952G= GRCh37
NC_000010.9:g.79409958G= NCBI36
NG_029648.1:g.54347C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000698724.1:n.1888C=
ENST00000698725.1:n.1641C=
ENST00000698726.1:n.3201C=
ENST00000698727.1:n.2934C=
ENST00000698728.1:n.3550C=
ENST00000698729.1:n.4998C=
ENST00000698730.1:n.5096C=
ENST00000698731.1:c.3830C= ENSP00000513898.1:p.Thr1277=
ENST00000698732.1:c.*2660C= ENSP00000513899.1:n.*2660C=
ENST00000698733.1:c.*3158C= ENSP00000513900.1:n.*3158C=
ENST00000698734.1:c.*2144C= ENSP00000513901.1:n.*2144C=
ENST00000698735.1:n.4322C=
ENST00000698736.1:n.4735C=
ENST00000698737.1:n.4086C=
ENST00000372371.8:c.3971C= MANE Select ENSP00000361446.3:p.Thr1324=
ENST00000372371.7:c.3971C= ENSP00000361446.3:p.Thr1324=
ENST00000616246.4:c.419C= ENSP00000483738.1:p.Thr140=
NM_007055.3:c.3971C= NP_008986.2:p.Thr1324=
NM_007055.4:c.3971C= MANE Select NP_008986.2:p.Thr1324=