Canonical Allele Identifier: CA377325943

Gene: POLR3A

Linked Data

• MyVariant Identifiers: chr10:g.79739909G>C (hg19) ; chr10:g.77980151G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.77980151G>C , CM000672.2:g.77980151G>C	GRCh38
NC_000010.10:g.79739909G>C , CM000672.1:g.79739909G>C	GRCh37
NC_000010.9:g.79409915G>C	NCBI36
NG_029648.1:g.54390C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698724.1:n.1931C>G
ENST00000698725.1:n.1684C>G
ENST00000698726.1:n.3244C>G
ENST00000698727.1:n.2977C>G
ENST00000698728.1:n.3593C>G
ENST00000698729.1:n.5041C>G
ENST00000698730.1:n.5139C>G
ENST00000698731.1:c.3873C>G	ENSP00000513898.1:p.Asp1291Glu
ENST00000698732.1:c.*2703C>G	ENSP00000513899.1:n.*2703C>G
ENST00000698733.1:c.*3201C>G	ENSP00000513900.1:n.*3201C>G
ENST00000698734.1:c.*2187C>G	ENSP00000513901.1:n.*2187C>G
ENST00000698735.1:n.4365C>G
ENST00000698736.1:n.4778C>G
ENST00000698737.1:n.4129C>G
ENST00000372371.8:c.4014C>G MANE Select	ENSP00000361446.3:p.Asp1338Glu
ENST00000372371.7:c.4014C>G	ENSP00000361446.3:p.Asp1338Glu
ENST00000616246.4:c.462C>G	ENSP00000483738.1:p.Asp154Glu
NM_007055.3:c.4014C>G	NP_008986.2:p.Asp1338Glu
NM_007055.4:c.4014C>G MANE Select	NP_008986.2:p.Asp1338Glu