Canonical Allele Identifier: CA377326077

Gene: POLR3A

Linked Data

• MyVariant Identifiers: chr10:g.79739967G>C (hg19) ; chr10:g.77980209G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.77980209G>C , CM000672.2:g.77980209G>C	GRCh38
NC_000010.10:g.79739967G>C , CM000672.1:g.79739967G>C	GRCh37
NC_000010.9:g.79409973G>C	NCBI36
NG_029648.1:g.54332C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698724.1:n.1873C>G
ENST00000698725.1:n.1626C>G
ENST00000698726.1:n.3186C>G
ENST00000698727.1:n.2919C>G
ENST00000698728.1:n.3535C>G
ENST00000698729.1:n.4983C>G
ENST00000698730.1:n.5081C>G
ENST00000698731.1:c.3815C>G	ENSP00000513898.1:p.Ala1272Gly
ENST00000698732.1:c.*2645C>G	ENSP00000513899.1:n.*2645C>G
ENST00000698733.1:c.*3143C>G	ENSP00000513900.1:n.*3143C>G
ENST00000698734.1:c.*2129C>G	ENSP00000513901.1:n.*2129C>G
ENST00000698735.1:n.4307C>G
ENST00000698736.1:n.4720C>G
ENST00000698737.1:n.4071C>G
ENST00000372371.8:c.3956C>G MANE Select	ENSP00000361446.3:p.Ala1319Gly
ENST00000372371.7:c.3956C>G	ENSP00000361446.3:p.Ala1319Gly
ENST00000616246.4:c.404C>G	ENSP00000483738.1:p.Ala135Gly
NM_007055.3:c.3956C>G	NP_008986.2:p.Ala1319Gly
NM_007055.4:c.3956C>G MANE Select	NP_008986.2:p.Ala1319Gly