Canonical Allele Identifier: CA377326160

Gene: POLR3A

Linked Data

• MyVariant Identifiers: chr10:g.79740004C>G (hg19) ; chr10:g.77980246C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.77980246C>G , CM000672.2:g.77980246C>G	GRCh38
NC_000010.10:g.79740004C>G , CM000672.1:g.79740004C>G	GRCh37
NC_000010.9:g.79410010C>G	NCBI36
NG_029648.1:g.54295G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698724.1:n.1836G>C
ENST00000698725.1:n.1589G>C
ENST00000698726.1:n.3149G>C
ENST00000698727.1:n.2882G>C
ENST00000698728.1:n.3498G>C
ENST00000698729.1:n.4946G>C
ENST00000698730.1:n.5044G>C
ENST00000698731.1:c.3778G>C	ENSP00000513898.1:p.Gly1260Arg
ENST00000698732.1:c.*2608G>C	ENSP00000513899.1:n.*2608G>C
ENST00000698733.1:c.*3106G>C	ENSP00000513900.1:n.*3106G>C
ENST00000698734.1:c.*2092G>C	ENSP00000513901.1:n.*2092G>C
ENST00000698735.1:n.4270G>C
ENST00000698736.1:n.4683G>C
ENST00000698737.1:n.4034G>C
ENST00000372371.8:c.3919G>C MANE Select	ENSP00000361446.3:p.Gly1307Arg
ENST00000372371.7:c.3919G>C	ENSP00000361446.3:p.Gly1307Arg
ENST00000616246.4:c.367G>C	ENSP00000483738.1:p.Gly123Arg
NM_007055.3:c.3919G>C	NP_008986.2:p.Gly1307Arg
NM_007055.4:c.3919G>C MANE Select	NP_008986.2:p.Gly1307Arg