Canonical Allele Identifier: CA470390650

Gene: POLR3A

Linked Data

• MyVariant Identifiers: chr10:g.79739954C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.77980196C>T , CM000672.2:g.77980196C>T	GRCh38
NC_000010.10:g.79739954C>T , CM000672.1:g.79739954C>T	GRCh37
NC_000010.9:g.79409960C>T	NCBI36
NG_029648.1:g.54345G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698724.1:n.1886G>A
ENST00000698725.1:n.1639G>A
ENST00000698726.1:n.3199G>A
ENST00000698727.1:n.2932G>A
ENST00000698728.1:n.3548G>A
ENST00000698729.1:n.4996G>A
ENST00000698730.1:n.5094G>A
ENST00000698731.1:c.3828G>A	ENSP00000513898.1:p.Lys1276=
ENST00000698732.1:c.*2658G>A	ENSP00000513899.1:n.*2658G>A
ENST00000698733.1:c.*3156G>A	ENSP00000513900.1:n.*3156G>A
ENST00000698734.1:c.*2142G>A	ENSP00000513901.1:n.*2142G>A
ENST00000698735.1:n.4320G>A
ENST00000698736.1:n.4733G>A
ENST00000698737.1:n.4084G>A
ENST00000372371.8:c.3969G>A MANE Select	ENSP00000361446.3:p.Lys1323=
ENST00000372371.7:c.3969G>A	ENSP00000361446.3:p.Lys1323=
ENST00000616246.4:c.417G>A	ENSP00000483738.1:p.Lys139=
NM_007055.3:c.3969G>A	NP_008986.2:p.Lys1323=
NM_007055.4:c.3969G>A MANE Select	NP_008986.2:p.Lys1323=