Canonical Allele Identifier: CA377325962

Gene: POLR3A

Linked Data

• MyVariant Identifiers: chr10:g.79739916T>G (hg19) ; chr10:g.77980158T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.77980158T>G , CM000672.2:g.77980158T>G	GRCh38
NC_000010.10:g.79739916T>G , CM000672.1:g.79739916T>G	GRCh37
NC_000010.9:g.79409922T>G	NCBI36
NG_029648.1:g.54383A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698724.1:n.1924A>C
ENST00000698725.1:n.1677A>C
ENST00000698726.1:n.3237A>C
ENST00000698727.1:n.2970A>C
ENST00000698728.1:n.3586A>C
ENST00000698729.1:n.5034A>C
ENST00000698730.1:n.5132A>C
ENST00000698731.1:c.3866A>C	ENSP00000513898.1:p.Gln1289Pro
ENST00000698732.1:c.*2696A>C	ENSP00000513899.1:n.*2696A>C
ENST00000698733.1:c.*3194A>C	ENSP00000513900.1:n.*3194A>C
ENST00000698734.1:c.*2180A>C	ENSP00000513901.1:n.*2180A>C
ENST00000698735.1:n.4358A>C
ENST00000698736.1:n.4771A>C
ENST00000698737.1:n.4122A>C
ENST00000372371.8:c.4007A>C MANE Select	ENSP00000361446.3:p.Gln1336Pro
ENST00000372371.7:c.4007A>C	ENSP00000361446.3:p.Gln1336Pro
ENST00000616246.4:c.455A>C	ENSP00000483738.1:p.Gln152Pro
NM_007055.3:c.4007A>C	NP_008986.2:p.Gln1336Pro
NM_007055.4:c.4007A>C MANE Select	NP_008986.2:p.Gln1336Pro