Canonical Allele Identifier: CA377326169

Gene: POLR3A

Linked Data

• MyVariant Identifiers: chr10:g.79740008C>A (hg19) ; chr10:g.77980250C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.77980250C>A , CM000672.2:g.77980250C>A	GRCh38
NC_000010.10:g.79740008C>A , CM000672.1:g.79740008C>A	GRCh37
NC_000010.9:g.79410014C>A	NCBI36
NG_029648.1:g.54291G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698724.1:n.1832G>T
ENST00000698725.1:n.1585G>T
ENST00000698726.1:n.3145G>T
ENST00000698727.1:n.2878G>T
ENST00000698728.1:n.3494G>T
ENST00000698729.1:n.4942G>T
ENST00000698730.1:n.5040G>T
ENST00000698731.1:c.3774G>T	ENSP00000513898.1:p.Arg1258Ser
ENST00000698732.1:c.*2604G>T	ENSP00000513899.1:n.*2604G>T
ENST00000698733.1:c.*3102G>T	ENSP00000513900.1:n.*3102G>T
ENST00000698734.1:c.*2088G>T	ENSP00000513901.1:n.*2088G>T
ENST00000698735.1:n.4266G>T
ENST00000698736.1:n.4679G>T
ENST00000698737.1:n.4030G>T
ENST00000372371.8:c.3915G>T MANE Select	ENSP00000361446.3:p.Arg1305Ser
ENST00000372371.7:c.3915G>T	ENSP00000361446.3:p.Arg1305Ser
ENST00000616246.4:c.363G>T	ENSP00000483738.1:p.Arg121Ser
NM_007055.3:c.3915G>T	NP_008986.2:p.Arg1305Ser
NM_007055.4:c.3915G>T MANE Select	NP_008986.2:p.Arg1305Ser