Canonical Allele Identifier: CA2574591844
Gene: POLR3A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.78010013A>G , CM000672.2:g.78010013A>G GRCh38
NC_000010.10:g.79769771A>G , CM000672.1:g.79769771A>G GRCh37
NC_000010.9:g.79439777A>G NCBI36
NG_029648.1:g.24528T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000698728.1:n.1222-22T>C
ENST00000698729.1:n.2768-22T>C
ENST00000698730.1:n.2768-22T>C
ENST00000698731.1:c.1502-22T>C ENSP00000513898.1:n.1502-22T>C
ENST00000698732.1:c.*504-22T>C ENSP00000513899.1:n.*504-22T>C
ENST00000698733.1:c.*830-22T>C ENSP00000513900.1:n.*830-22T>C
ENST00000698734.1:c.1643-22T>C ENSP00000513901.1:n.1643-22T>C
ENST00000698735.1:n.1758-22T>C
ENST00000698736.1:n.1758-22T>C
ENST00000698737.1:n.1758-22T>C
ENST00000698738.1:n.1758-22T>C
ENST00000698739.1:n.1758-22T>C
ENST00000372371.8:c.1643-22T>C MANE Select ENSP00000361446.3:n.1643-22T>C
ENST00000372371.7:c.1643-22T>C ENSP00000361446.3:n.1643-22T>C
ENST00000473588.2:c.445-22T>C
NM_007055.3:c.1643-22T>C NP_008986.2:n.1643-22T>C
NM_007055.4:c.1643-22T>C MANE Select NP_008986.2:n.1643-22T>C