Canonical Allele Identifier: CA1921497507
Gene: POLR3A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.77980193C= , CM000672.2:g.77980193C= GRCh38
NC_000010.10:g.79739951C= , CM000672.1:g.79739951C= GRCh37
NC_000010.9:g.79409957C= NCBI36
NG_029648.1:g.54348G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000698724.1:n.1889G=
ENST00000698725.1:n.1642G=
ENST00000698726.1:n.3202G=
ENST00000698727.1:n.2935G=
ENST00000698728.1:n.3551G=
ENST00000698729.1:n.4999G=
ENST00000698730.1:n.5097G=
ENST00000698731.1:c.3831G= ENSP00000513898.1:p.Thr1277=
ENST00000698732.1:c.*2661G= ENSP00000513899.1:n.*2661G=
ENST00000698733.1:c.*3159G= ENSP00000513900.1:n.*3159G=
ENST00000698734.1:c.*2145G= ENSP00000513901.1:n.*2145G=
ENST00000698735.1:n.4323G=
ENST00000698736.1:n.4736G=
ENST00000698737.1:n.4087G=
ENST00000372371.8:c.3972G= MANE Select ENSP00000361446.3:p.Thr1324=
ENST00000372371.7:c.3972G= ENSP00000361446.3:p.Thr1324=
ENST00000616246.4:c.420G= ENSP00000483738.1:p.Thr140=
NM_007055.3:c.3972G= NP_008986.2:p.Thr1324=
NM_007055.4:c.3972G= MANE Select NP_008986.2:p.Thr1324=