Canonical Allele Identifier: CA1921497494
Gene: POLR3A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.77980153C= , CM000672.2:g.77980153C= GRCh38
NC_000010.10:g.79739911C= , CM000672.1:g.79739911C= GRCh37
NC_000010.9:g.79409917C= NCBI36
NG_029648.1:g.54388G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000698724.1:n.1929G=
ENST00000698725.1:n.1682G=
ENST00000698726.1:n.3242G=
ENST00000698727.1:n.2975G=
ENST00000698728.1:n.3591G=
ENST00000698729.1:n.5039G=
ENST00000698730.1:n.5137G=
ENST00000698731.1:c.3871G= ENSP00000513898.1:p.Asp1291=
ENST00000698732.1:c.*2701G= ENSP00000513899.1:n.*2701G=
ENST00000698733.1:c.*3199G= ENSP00000513900.1:n.*3199G=
ENST00000698734.1:c.*2185G= ENSP00000513901.1:n.*2185G=
ENST00000698735.1:n.4363G=
ENST00000698736.1:n.4776G=
ENST00000698737.1:n.4127G=
ENST00000372371.8:c.4012G= MANE Select ENSP00000361446.3:p.Asp1338=
ENST00000372371.7:c.4012G= ENSP00000361446.3:p.Asp1338=
ENST00000616246.4:c.460G= ENSP00000483738.1:p.Asp154=
NM_007055.3:c.4012G= NP_008986.2:p.Asp1338=
NM_007055.4:c.4012G= MANE Select NP_008986.2:p.Asp1338=