Canonical Allele Identifier: CA377325968

Gene: POLR3A

Linked Data

• MyVariant Identifiers: chr10:g.79739919C>T (hg19) ; chr10:g.77980161C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.77980161C>T , CM000672.2:g.77980161C>T	GRCh38
NC_000010.10:g.79739919C>T , CM000672.1:g.79739919C>T	GRCh37
NC_000010.9:g.79409925C>T	NCBI36
NG_029648.1:g.54380G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698724.1:n.1921G>A
ENST00000698725.1:n.1674G>A
ENST00000698726.1:n.3234G>A
ENST00000698727.1:n.2967G>A
ENST00000698728.1:n.3583G>A
ENST00000698729.1:n.5031G>A
ENST00000698730.1:n.5129G>A
ENST00000698731.1:c.3863G>A	ENSP00000513898.1:p.Gly1288Glu
ENST00000698732.1:c.*2693G>A	ENSP00000513899.1:n.*2693G>A
ENST00000698733.1:c.*3191G>A	ENSP00000513900.1:n.*3191G>A
ENST00000698734.1:c.*2177G>A	ENSP00000513901.1:n.*2177G>A
ENST00000698735.1:n.4355G>A
ENST00000698736.1:n.4768G>A
ENST00000698737.1:n.4119G>A
ENST00000372371.8:c.4004G>A MANE Select	ENSP00000361446.3:p.Gly1335Glu
ENST00000372371.7:c.4004G>A	ENSP00000361446.3:p.Gly1335Glu
ENST00000616246.4:c.452G>A	ENSP00000483738.1:p.Gly151Glu
NM_007055.3:c.4004G>A	NP_008986.2:p.Gly1335Glu
NM_007055.4:c.4004G>A MANE Select	NP_008986.2:p.Gly1335Glu