Canonical Allele Identifier: CA377337933

Gene: POLR3A

Linked Data

• MyVariant Identifiers: chr10:g.79764497A>G (hg19) ; chr10:g.78004739A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.78004739A>G , CM000672.2:g.78004739A>G	GRCh38
NC_000010.10:g.79764497A>G , CM000672.1:g.79764497A>G	GRCh37
NC_000010.9:g.79434503A>G	NCBI36
NG_029648.1:g.29802T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698727.1:n.1284T>C
ENST00000698728.1:n.1803T>C
ENST00000698729.1:n.3349T>C
ENST00000698730.1:n.3349T>C
ENST00000698731.1:c.2083T>C	ENSP00000513898.1:p.Cys695Arg
ENST00000698732.1:c.*1085T>C	ENSP00000513899.1:n.*1085T>C
ENST00000698733.1:c.*1411T>C	ENSP00000513900.1:n.*1411T>C
ENST00000698734.1:c.2224T>C	ENSP00000513901.1:p.Cys742Arg
ENST00000698735.1:n.2339T>C
ENST00000698736.1:n.2339T>C
ENST00000698737.1:n.2339T>C
ENST00000698738.1:n.2339T>C
ENST00000698739.1:n.2339T>C
ENST00000372371.8:c.2224T>C MANE Select	ENSP00000361446.3:p.Cys742Arg
ENST00000372371.7:c.2224T>C	ENSP00000361446.3:p.Cys742Arg
ENST00000472014.5:n.446T>C
ENST00000473588.2:c.887T>C
NM_007055.3:c.2224T>C	NP_008986.2:p.Cys742Arg
NM_007055.4:c.2224T>C MANE Select	NP_008986.2:p.Cys742Arg