Canonical Allele Identifier: CA1921495598
Gene: POLR3A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.77975816C= , CM000672.2:g.77975816C= GRCh38
NC_000010.10:g.79735574C= , CM000672.1:g.79735574C= GRCh37
NC_000010.9:g.79405580C= NCBI36
NG_029648.1:g.58725G=

Transcript Alleles

HGVS Amino-acid change
ENST00000698724.1:n.1941+4325G=
ENST00000698725.1:n.3505G=
ENST00000698726.1:n.5065G=
ENST00000698727.1:n.4798G=
ENST00000698728.1:n.5414G=
ENST00000698729.1:n.6862G=
ENST00000698730.1:n.6960G=
ENST00000698731.1:c.*1662G= ENSP00000513898.1:n.*1662G=
ENST00000698732.1:c.*4524G= ENSP00000513899.1:n.*4524G=
ENST00000698733.1:c.*5022G= ENSP00000513900.1:n.*5022G=
ENST00000698734.1:c.*4008G= ENSP00000513901.1:n.*4008G=
ENST00000698735.1:n.6186G=
ENST00000698736.1:n.6599G=
ENST00000372371.8:c.*1662G= MANE Select ENSP00000361446.3:n.*1662G=
ENST00000372371.7:c.*1662G= ENSP00000361446.3:n.*1662G=
ENST00000616246.4:c.472+4325G= ENSP00000483738.1:n.472+4325G=
NM_007055.3:c.*1662G= NP_008986.2:n.*1662G=
NM_007055.4:c.*1662G= MANE Select NP_008986.2:n.*1662G=