Canonical Allele Identifier: CA470390696

Gene: POLR3A

Linked Data

• MyVariant Identifiers: chr10:g.79740023G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.77980265G>C , CM000672.2:g.77980265G>C	GRCh38
NC_000010.10:g.79740023G>C , CM000672.1:g.79740023G>C	GRCh37
NC_000010.9:g.79410029G>C	NCBI36
NG_029648.1:g.54276C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698724.1:n.1817C>G
ENST00000698725.1:n.1570C>G
ENST00000698726.1:n.3130C>G
ENST00000698727.1:n.2863C>G
ENST00000698728.1:n.3479C>G
ENST00000698729.1:n.4927C>G
ENST00000698730.1:n.5025C>G
ENST00000698731.1:c.3759C>G	ENSP00000513898.1:p.Val1253=
ENST00000698732.1:c.*2589C>G	ENSP00000513899.1:n.*2589C>G
ENST00000698733.1:c.*3087C>G	ENSP00000513900.1:n.*3087C>G
ENST00000698734.1:c.*2073C>G	ENSP00000513901.1:n.*2073C>G
ENST00000698735.1:n.4251C>G
ENST00000698736.1:n.4664C>G
ENST00000698737.1:n.4015C>G
ENST00000372371.8:c.3900C>G MANE Select	ENSP00000361446.3:p.Val1300=
ENST00000372371.7:c.3900C>G	ENSP00000361446.3:p.Val1300=
ENST00000616246.4:c.348C>G	ENSP00000483738.1:p.Val116=
NM_007055.3:c.3900C>G	NP_008986.2:p.Val1300=
NM_007055.4:c.3900C>G MANE Select	NP_008986.2:p.Val1300=