Canonical Allele Identifier: CA377325994

Gene: POLR3A

Linked Data

• MyVariant Identifiers: chr10:g.79739931G>C (hg19) ; chr10:g.77980173G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.77980173G>C , CM000672.2:g.77980173G>C	GRCh38
NC_000010.10:g.79739931G>C , CM000672.1:g.79739931G>C	GRCh37
NC_000010.9:g.79409937G>C	NCBI36
NG_029648.1:g.54368C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698724.1:n.1909C>G
ENST00000698725.1:n.1662C>G
ENST00000698726.1:n.3222C>G
ENST00000698727.1:n.2955C>G
ENST00000698728.1:n.3571C>G
ENST00000698729.1:n.5019C>G
ENST00000698730.1:n.5117C>G
ENST00000698731.1:c.3851C>G	ENSP00000513898.1:p.Ala1284Gly
ENST00000698732.1:c.*2681C>G	ENSP00000513899.1:n.*2681C>G
ENST00000698733.1:c.*3179C>G	ENSP00000513900.1:n.*3179C>G
ENST00000698734.1:c.*2165C>G	ENSP00000513901.1:n.*2165C>G
ENST00000698735.1:n.4343C>G
ENST00000698736.1:n.4756C>G
ENST00000698737.1:n.4107C>G
ENST00000372371.8:c.3992C>G MANE Select	ENSP00000361446.3:p.Ala1331Gly
ENST00000372371.7:c.3992C>G	ENSP00000361446.3:p.Ala1331Gly
ENST00000616246.4:c.440C>G	ENSP00000483738.1:p.Ala147Gly
NM_007055.3:c.3992C>G	NP_008986.2:p.Ala1331Gly
NM_007055.4:c.3992C>G MANE Select	NP_008986.2:p.Ala1331Gly