Canonical Allele Identifier: CA377325964

Gene: POLR3A

Linked Data

• MyVariant Identifiers: chr10:g.79739917G>C (hg19) ; chr10:g.77980159G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.77980159G>C , CM000672.2:g.77980159G>C	GRCh38
NC_000010.10:g.79739917G>C , CM000672.1:g.79739917G>C	GRCh37
NC_000010.9:g.79409923G>C	NCBI36
NG_029648.1:g.54382C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698724.1:n.1923C>G
ENST00000698725.1:n.1676C>G
ENST00000698726.1:n.3236C>G
ENST00000698727.1:n.2969C>G
ENST00000698728.1:n.3585C>G
ENST00000698729.1:n.5033C>G
ENST00000698730.1:n.5131C>G
ENST00000698731.1:c.3865C>G	ENSP00000513898.1:p.Gln1289Glu
ENST00000698732.1:c.*2695C>G	ENSP00000513899.1:n.*2695C>G
ENST00000698733.1:c.*3193C>G	ENSP00000513900.1:n.*3193C>G
ENST00000698734.1:c.*2179C>G	ENSP00000513901.1:n.*2179C>G
ENST00000698735.1:n.4357C>G
ENST00000698736.1:n.4770C>G
ENST00000698737.1:n.4121C>G
ENST00000372371.8:c.4006C>G MANE Select	ENSP00000361446.3:p.Gln1336Glu
ENST00000372371.7:c.4006C>G	ENSP00000361446.3:p.Gln1336Glu
ENST00000616246.4:c.454C>G	ENSP00000483738.1:p.Gln152Glu
NM_007055.3:c.4006C>G	NP_008986.2:p.Gln1336Glu
NM_007055.4:c.4006C>G MANE Select	NP_008986.2:p.Gln1336Glu