Canonical Allele Identifier: CA470390689

Gene: POLR3A

Linked Data

• MyVariant Identifiers: chr10:g.79740017G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.77980259G>C , CM000672.2:g.77980259G>C	GRCh38
NC_000010.10:g.79740017G>C , CM000672.1:g.79740017G>C	GRCh37
NC_000010.9:g.79410023G>C	NCBI36
NG_029648.1:g.54282C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698724.1:n.1823C>G
ENST00000698725.1:n.1576C>G
ENST00000698726.1:n.3136C>G
ENST00000698727.1:n.2869C>G
ENST00000698728.1:n.3485C>G
ENST00000698729.1:n.4933C>G
ENST00000698730.1:n.5031C>G
ENST00000698731.1:c.3765C>G	ENSP00000513898.1:p.Gly1255=
ENST00000698732.1:c.*2595C>G	ENSP00000513899.1:n.*2595C>G
ENST00000698733.1:c.*3093C>G	ENSP00000513900.1:n.*3093C>G
ENST00000698734.1:c.*2079C>G	ENSP00000513901.1:n.*2079C>G
ENST00000698735.1:n.4257C>G
ENST00000698736.1:n.4670C>G
ENST00000698737.1:n.4021C>G
ENST00000372371.8:c.3906C>G MANE Select	ENSP00000361446.3:p.Gly1302=
ENST00000372371.7:c.3906C>G	ENSP00000361446.3:p.Gly1302=
ENST00000616246.4:c.354C>G	ENSP00000483738.1:p.Gly118=
NM_007055.3:c.3906C>G	NP_008986.2:p.Gly1302=
NM_007055.4:c.3906C>G MANE Select	NP_008986.2:p.Gly1302=