Canonical Allele Identifier: CA1921497454
Gene: POLR3A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.77980084G= , CM000672.2:g.77980084G= GRCh38
NC_000010.10:g.79739842G= , CM000672.1:g.79739842G= GRCh37
NC_000010.9:g.79409848G= NCBI36
NG_029648.1:g.54457C=

Transcript Alleles

HGVS Amino-acid change
ENST00000698724.1:n.1941+57C=
ENST00000698725.1:n.1694+57C=
ENST00000698726.1:n.3254+57C=
ENST00000698727.1:n.2987+57C=
ENST00000698728.1:n.3603+57C=
ENST00000698729.1:n.5051+57C=
ENST00000698730.1:n.5149+57C=
ENST00000698731.1:c.3883+57C= ENSP00000513898.1:n.3883+57C=
ENST00000698732.1:c.*2713+57C= ENSP00000513899.1:n.*2713+57C=
ENST00000698733.1:c.*3211+57C= ENSP00000513900.1:n.*3211+57C=
ENST00000698734.1:c.*2197+57C= ENSP00000513901.1:n.*2197+57C=
ENST00000698735.1:n.4375+57C=
ENST00000698736.1:n.4788+57C=
ENST00000698737.1:n.4196C=
ENST00000372371.8:c.4024+57C= MANE Select ENSP00000361446.3:n.4024+57C=
ENST00000372371.7:c.4024+57C= ENSP00000361446.3:n.4024+57C=
ENST00000616246.4:c.472+57C= ENSP00000483738.1:n.472+57C=
NM_007055.3:c.4024+57C= NP_008986.2:n.4024+57C=
NM_007055.4:c.4024+57C= MANE Select NP_008986.2:n.4024+57C=