Canonical Allele Identifier: CA470390656

Gene: POLR3A

Linked Data

• MyVariant Identifiers: chr10:g.79739966G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.77980208G>C , CM000672.2:g.77980208G>C	GRCh38
NC_000010.10:g.79739966G>C , CM000672.1:g.79739966G>C	GRCh37
NC_000010.9:g.79409972G>C	NCBI36
NG_029648.1:g.54333C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698724.1:n.1874C>G
ENST00000698725.1:n.1627C>G
ENST00000698726.1:n.3187C>G
ENST00000698727.1:n.2920C>G
ENST00000698728.1:n.3536C>G
ENST00000698729.1:n.4984C>G
ENST00000698730.1:n.5082C>G
ENST00000698731.1:c.3816C>G	ENSP00000513898.1:p.Ala1272=
ENST00000698732.1:c.*2646C>G	ENSP00000513899.1:n.*2646C>G
ENST00000698733.1:c.*3144C>G	ENSP00000513900.1:n.*3144C>G
ENST00000698734.1:c.*2130C>G	ENSP00000513901.1:n.*2130C>G
ENST00000698735.1:n.4308C>G
ENST00000698736.1:n.4721C>G
ENST00000698737.1:n.4072C>G
ENST00000372371.8:c.3957C>G MANE Select	ENSP00000361446.3:p.Ala1319=
ENST00000372371.7:c.3957C>G	ENSP00000361446.3:p.Ala1319=
ENST00000616246.4:c.405C>G	ENSP00000483738.1:p.Ala135=
NM_007055.3:c.3957C>G	NP_008986.2:p.Ala1319=
NM_007055.4:c.3957C>G MANE Select	NP_008986.2:p.Ala1319=