Canonical Allele Identifier: CA377325984

Gene: POLR3A

Linked Data

• MyVariant Identifiers: chr10:g.79739926A>C (hg19) ; chr10:g.77980168A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.77980168A>C , CM000672.2:g.77980168A>C	GRCh38
NC_000010.10:g.79739926A>C , CM000672.1:g.79739926A>C	GRCh37
NC_000010.9:g.79409932A>C	NCBI36
NG_029648.1:g.54373T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698724.1:n.1914T>G
ENST00000698725.1:n.1667T>G
ENST00000698726.1:n.3227T>G
ENST00000698727.1:n.2960T>G
ENST00000698728.1:n.3576T>G
ENST00000698729.1:n.5024T>G
ENST00000698730.1:n.5122T>G
ENST00000698731.1:c.3856T>G	ENSP00000513898.1:p.Tyr1286Asp
ENST00000698732.1:c.*2686T>G	ENSP00000513899.1:n.*2686T>G
ENST00000698733.1:c.*3184T>G	ENSP00000513900.1:n.*3184T>G
ENST00000698734.1:c.*2170T>G	ENSP00000513901.1:n.*2170T>G
ENST00000698735.1:n.4348T>G
ENST00000698736.1:n.4761T>G
ENST00000698737.1:n.4112T>G
ENST00000372371.8:c.3997T>G MANE Select	ENSP00000361446.3:p.Tyr1333Asp
ENST00000372371.7:c.3997T>G	ENSP00000361446.3:p.Tyr1333Asp
ENST00000616246.4:c.445T>G	ENSP00000483738.1:p.Tyr149Asp
NM_007055.3:c.3997T>G	NP_008986.2:p.Tyr1333Asp
NM_007055.4:c.3997T>G MANE Select	NP_008986.2:p.Tyr1333Asp