Canonical Allele Identifier: CA470390652

Gene: POLR3A

Linked Data

• MyVariant Identifiers: chr10:g.79739960A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.77980202A>G , CM000672.2:g.77980202A>G	GRCh38
NC_000010.10:g.79739960A>G , CM000672.1:g.79739960A>G	GRCh37
NC_000010.9:g.79409966A>G	NCBI36
NG_029648.1:g.54339T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698724.1:n.1880T>C
ENST00000698725.1:n.1633T>C
ENST00000698726.1:n.3193T>C
ENST00000698727.1:n.2926T>C
ENST00000698728.1:n.3542T>C
ENST00000698729.1:n.4990T>C
ENST00000698730.1:n.5088T>C
ENST00000698731.1:c.3822T>C	ENSP00000513898.1:p.Phe1274=
ENST00000698732.1:c.*2652T>C	ENSP00000513899.1:n.*2652T>C
ENST00000698733.1:c.*3150T>C	ENSP00000513900.1:n.*3150T>C
ENST00000698734.1:c.*2136T>C	ENSP00000513901.1:n.*2136T>C
ENST00000698735.1:n.4314T>C
ENST00000698736.1:n.4727T>C
ENST00000698737.1:n.4078T>C
ENST00000372371.8:c.3963T>C MANE Select	ENSP00000361446.3:p.Phe1321=
ENST00000372371.7:c.3963T>C	ENSP00000361446.3:p.Phe1321=
ENST00000616246.4:c.411T>C	ENSP00000483738.1:p.Phe137=
NM_007055.3:c.3963T>C	NP_008986.2:p.Phe1321=
NM_007055.4:c.3963T>C MANE Select	NP_008986.2:p.Phe1321=