Canonical Allele Identifier: CA377326173

Gene: POLR3A

Linked Data

• MyVariant Identifiers: chr10:g.79740009C>G (hg19) ; chr10:g.77980251C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.77980251C>G , CM000672.2:g.77980251C>G	GRCh38
NC_000010.10:g.79740009C>G , CM000672.1:g.79740009C>G	GRCh37
NC_000010.9:g.79410015C>G	NCBI36
NG_029648.1:g.54290G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698724.1:n.1831G>C
ENST00000698725.1:n.1584G>C
ENST00000698726.1:n.3144G>C
ENST00000698727.1:n.2877G>C
ENST00000698728.1:n.3493G>C
ENST00000698729.1:n.4941G>C
ENST00000698730.1:n.5039G>C
ENST00000698731.1:c.3773G>C	ENSP00000513898.1:p.Arg1258Thr
ENST00000698732.1:c.*2603G>C	ENSP00000513899.1:n.*2603G>C
ENST00000698733.1:c.*3101G>C	ENSP00000513900.1:n.*3101G>C
ENST00000698734.1:c.*2087G>C	ENSP00000513901.1:n.*2087G>C
ENST00000698735.1:n.4265G>C
ENST00000698736.1:n.4678G>C
ENST00000698737.1:n.4029G>C
ENST00000372371.8:c.3914G>C MANE Select	ENSP00000361446.3:p.Arg1305Thr
ENST00000372371.7:c.3914G>C	ENSP00000361446.3:p.Arg1305Thr
ENST00000616246.4:c.362G>C	ENSP00000483738.1:p.Arg121Thr
NM_007055.3:c.3914G>C	NP_008986.2:p.Arg1305Thr
NM_007055.4:c.3914G>C MANE Select	NP_008986.2:p.Arg1305Thr