Canonical Allele Identifier: CA377325979
Gene: POLR3A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.77980166G>C , CM000672.2:g.77980166G>C GRCh38
NC_000010.10:g.79739924G>C , CM000672.1:g.79739924G>C GRCh37
NC_000010.9:g.79409930G>C NCBI36
NG_029648.1:g.54375C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000698724.1:n.1916C>G
ENST00000698725.1:n.1669C>G
ENST00000698726.1:n.3229C>G
ENST00000698727.1:n.2962C>G
ENST00000698728.1:n.3578C>G
ENST00000698729.1:n.5026C>G
ENST00000698730.1:n.5124C>G
ENST00000698731.1:c.3858C>G ENSP00000513898.1:p.Tyr1286Ter
ENST00000698732.1:c.*2688C>G ENSP00000513899.1:n.*2688C>G
ENST00000698733.1:c.*3186C>G ENSP00000513900.1:n.*3186C>G
ENST00000698734.1:c.*2172C>G ENSP00000513901.1:n.*2172C>G
ENST00000698735.1:n.4350C>G
ENST00000698736.1:n.4763C>G
ENST00000698737.1:n.4114C>G
ENST00000372371.8:c.3999C>G MANE Select ENSP00000361446.3:p.Tyr1333Ter
ENST00000372371.7:c.3999C>G ENSP00000361446.3:p.Tyr1333Ter
ENST00000616246.4:c.447C>G ENSP00000483738.1:p.Tyr149Ter
NM_007055.3:c.3999C>G NP_008986.2:p.Tyr1333Ter
NM_007055.4:c.3999C>G MANE Select NP_008986.2:p.Tyr1333Ter