Canonical Allele Identifier: CA1921497433
Gene: POLR3A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.77980014T= , CM000672.2:g.77980014T= GRCh38
NC_000010.10:g.79739772T= , CM000672.1:g.79739772T= GRCh37
NC_000010.9:g.79409778T= NCBI36
NG_029648.1:g.54527A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000698724.1:n.1941+127A=
ENST00000698725.1:n.1694+127A=
ENST00000698726.1:n.3254+127A=
ENST00000698727.1:n.2987+127A=
ENST00000698728.1:n.3603+127A=
ENST00000698729.1:n.5051+127A=
ENST00000698730.1:n.5149+127A=
ENST00000698731.1:c.3883+127A= ENSP00000513898.1:n.3883+127A=
ENST00000698732.1:c.*2713+127A= ENSP00000513899.1:n.*2713+127A=
ENST00000698733.1:c.*3211+127A= ENSP00000513900.1:n.*3211+127A=
ENST00000698734.1:c.*2197+127A= ENSP00000513901.1:n.*2197+127A=
ENST00000698735.1:n.4375+127A=
ENST00000698736.1:n.4788+127A=
ENST00000372371.8:c.4024+127A= MANE Select ENSP00000361446.3:n.4024+127A=
ENST00000372371.7:c.4024+127A= ENSP00000361446.3:n.4024+127A=
ENST00000616246.4:c.472+127A= ENSP00000483738.1:n.472+127A=
NM_007055.3:c.4024+127A= NP_008986.2:n.4024+127A=
NM_007055.4:c.4024+127A= MANE Select NP_008986.2:n.4024+127A=