Canonical Allele Identifier: CA377325966

Gene: POLR3A

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698724.1:n.1921G>T
ENST00000698725.1:n.1674G>T
ENST00000698726.1:n.3234G>T
ENST00000698727.1:n.2967G>T
ENST00000698728.1:n.3583G>T
ENST00000698729.1:n.5031G>T
ENST00000698730.1:n.5129G>T
ENST00000698731.1:c.3863G>T	ENSP00000513898.1:p.Gly1288Val
ENST00000698732.1:c.*2693G>T	ENSP00000513899.1:n.*2693G>T
ENST00000698733.1:c.*3191G>T	ENSP00000513900.1:n.*3191G>T
ENST00000698734.1:c.*2177G>T	ENSP00000513901.1:n.*2177G>T
ENST00000698735.1:n.4355G>T
ENST00000698736.1:n.4768G>T
ENST00000698737.1:n.4119G>T
ENST00000372371.8:c.4004G>T MANE Select	ENSP00000361446.3:p.Gly1335Val
ENST00000372371.7:c.4004G>T	ENSP00000361446.3:p.Gly1335Val
ENST00000616246.4:c.452G>T	ENSP00000483738.1:p.Gly151Val
NM_007055.3:c.4004G>T	NP_008986.2:p.Gly1335Val
NM_007055.4:c.4004G>T MANE Select	NP_008986.2:p.Gly1335Val