Canonical Allele Identifier: CA470390666

Gene: POLR3A

Linked Data

• MyVariant Identifiers: chr10:g.79739978C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.77980220C>T , CM000672.2:g.77980220C>T	GRCh38
NC_000010.10:g.79739978C>T , CM000672.1:g.79739978C>T	GRCh37
NC_000010.9:g.79409984C>T	NCBI36
NG_029648.1:g.54321G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698724.1:n.1862G>A
ENST00000698725.1:n.1615G>A
ENST00000698726.1:n.3175G>A
ENST00000698727.1:n.2908G>A
ENST00000698728.1:n.3524G>A
ENST00000698729.1:n.4972G>A
ENST00000698730.1:n.5070G>A
ENST00000698731.1:c.3804G>A	ENSP00000513898.1:p.Val1268=
ENST00000698732.1:c.*2634G>A	ENSP00000513899.1:n.*2634G>A
ENST00000698733.1:c.*3132G>A	ENSP00000513900.1:n.*3132G>A
ENST00000698734.1:c.*2118G>A	ENSP00000513901.1:n.*2118G>A
ENST00000698735.1:n.4296G>A
ENST00000698736.1:n.4709G>A
ENST00000698737.1:n.4060G>A
ENST00000372371.8:c.3945G>A MANE Select	ENSP00000361446.3:p.Val1315=
ENST00000372371.7:c.3945G>A	ENSP00000361446.3:p.Val1315=
ENST00000616246.4:c.393G>A	ENSP00000483738.1:p.Val131=
NM_007055.3:c.3945G>A	NP_008986.2:p.Val1315=
NM_007055.4:c.3945G>A MANE Select	NP_008986.2:p.Val1315=