Canonical Allele Identifier: CA377326059

Gene: POLR3A

Linked Data

• MyVariant Identifiers: chr10:g.79739959C>G (hg19) ; chr10:g.77980201C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.77980201C>G , CM000672.2:g.77980201C>G	GRCh38
NC_000010.10:g.79739959C>G , CM000672.1:g.79739959C>G	GRCh37
NC_000010.9:g.79409965C>G	NCBI36
NG_029648.1:g.54340G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698724.1:n.1881G>C
ENST00000698725.1:n.1634G>C
ENST00000698726.1:n.3194G>C
ENST00000698727.1:n.2927G>C
ENST00000698728.1:n.3543G>C
ENST00000698729.1:n.4991G>C
ENST00000698730.1:n.5089G>C
ENST00000698731.1:c.3823G>C	ENSP00000513898.1:p.Glu1275Gln
ENST00000698732.1:c.*2653G>C	ENSP00000513899.1:n.*2653G>C
ENST00000698733.1:c.*3151G>C	ENSP00000513900.1:n.*3151G>C
ENST00000698734.1:c.*2137G>C	ENSP00000513901.1:n.*2137G>C
ENST00000698735.1:n.4315G>C
ENST00000698736.1:n.4728G>C
ENST00000698737.1:n.4079G>C
ENST00000372371.8:c.3964G>C MANE Select	ENSP00000361446.3:p.Glu1322Gln
ENST00000372371.7:c.3964G>C	ENSP00000361446.3:p.Glu1322Gln
ENST00000616246.4:c.412G>C	ENSP00000483738.1:p.Glu138Gln
NM_007055.3:c.3964G>C	NP_008986.2:p.Glu1322Gln
NM_007055.4:c.3964G>C MANE Select	NP_008986.2:p.Glu1322Gln