Canonical Allele Identifier: CA377326008

Gene: POLR3A

Linked Data

• MyVariant Identifiers: chr10:g.79739937A>C (hg19) ; chr10:g.77980179A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.77980179A>C , CM000672.2:g.77980179A>C	GRCh38
NC_000010.10:g.79739937A>C , CM000672.1:g.79739937A>C	GRCh37
NC_000010.9:g.79409943A>C	NCBI36
NG_029648.1:g.54362T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698724.1:n.1903T>G
ENST00000698725.1:n.1656T>G
ENST00000698726.1:n.3216T>G
ENST00000698727.1:n.2949T>G
ENST00000698728.1:n.3565T>G
ENST00000698729.1:n.5013T>G
ENST00000698730.1:n.5111T>G
ENST00000698731.1:c.3845T>G	ENSP00000513898.1:p.Phe1282Cys
ENST00000698732.1:c.*2675T>G	ENSP00000513899.1:n.*2675T>G
ENST00000698733.1:c.*3173T>G	ENSP00000513900.1:n.*3173T>G
ENST00000698734.1:c.*2159T>G	ENSP00000513901.1:n.*2159T>G
ENST00000698735.1:n.4337T>G
ENST00000698736.1:n.4750T>G
ENST00000698737.1:n.4101T>G
ENST00000372371.8:c.3986T>G MANE Select	ENSP00000361446.3:p.Phe1329Cys
ENST00000372371.7:c.3986T>G	ENSP00000361446.3:p.Phe1329Cys
ENST00000616246.4:c.434T>G	ENSP00000483738.1:p.Phe145Cys
NM_007055.3:c.3986T>G	NP_008986.2:p.Phe1329Cys
NM_007055.4:c.3986T>G MANE Select	NP_008986.2:p.Phe1329Cys