Canonical Allele Identifier: CA377335421

Gene: POLR3A

Linked Data

• MyVariant Identifiers: chr10:g.79759749C>A (hg19) ; chr10:g.77999991C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.77999991C>A , CM000672.2:g.77999991C>A	GRCh38
NC_000010.10:g.79759749C>A , CM000672.1:g.79759749C>A	GRCh37
NC_000010.9:g.79429755C>A	NCBI36
NG_029648.1:g.34550G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698727.1:n.1666G>T
ENST00000698728.1:n.2185G>T
ENST00000698729.1:n.3731G>T
ENST00000698730.1:n.3731G>T
ENST00000698731.1:c.2465G>T	ENSP00000513898.1:p.Gly822Val
ENST00000698732.1:c.*1467G>T	ENSP00000513899.1:n.*1467G>T
ENST00000698733.1:c.*1793G>T	ENSP00000513900.1:n.*1793G>T
ENST00000698734.1:c.2606G>T	ENSP00000513901.1:p.Gly869Val
ENST00000698735.1:n.2721G>T
ENST00000698736.1:n.2721G>T
ENST00000698737.1:n.2721G>T
ENST00000698738.1:n.2721G>T
ENST00000698739.1:n.2721G>T
ENST00000372371.8:c.2606G>T MANE Select	ENSP00000361446.3:p.Gly869Val
ENST00000372371.7:c.2606G>T	ENSP00000361446.3:p.Gly869Val
ENST00000472014.5:n.469+4725G>T
NM_007055.3:c.2606G>T	NP_008986.2:p.Gly869Val
NM_007055.4:c.2606G>T MANE Select	NP_008986.2:p.Gly869Val