Canonical Allele Identifier: CA470390670

Gene: POLR3A

Linked Data

• dbSNP Id: rs1254939674
• MyVariant Identifiers: chr10:g.79739993C>T (hg19) ; chr10:g.77980235C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.77980235C>T , CM000672.2:g.77980235C>T	GRCh38
NC_000010.10:g.79739993C>T , CM000672.1:g.79739993C>T	GRCh37
NC_000010.9:g.79409999C>T	NCBI36
NG_029648.1:g.54306G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698724.1:n.1847G>A
ENST00000698725.1:n.1600G>A
ENST00000698726.1:n.3160G>A
ENST00000698727.1:n.2893G>A
ENST00000698728.1:n.3509G>A
ENST00000698729.1:n.4957G>A
ENST00000698730.1:n.5055G>A
ENST00000698731.1:c.3789G>A	ENSP00000513898.1:p.Lys1263=
ENST00000698732.1:c.*2619G>A	ENSP00000513899.1:n.*2619G>A
ENST00000698733.1:c.*3117G>A	ENSP00000513900.1:n.*3117G>A
ENST00000698734.1:c.*2103G>A	ENSP00000513901.1:n.*2103G>A
ENST00000698735.1:n.4281G>A
ENST00000698736.1:n.4694G>A
ENST00000698737.1:n.4045G>A
ENST00000372371.8:c.3930G>A MANE Select	ENSP00000361446.3:p.Lys1310=
ENST00000372371.7:c.3930G>A	ENSP00000361446.3:p.Lys1310=
ENST00000616246.4:c.378G>A	ENSP00000483738.1:p.Lys126=
NM_007055.3:c.3930G>A	NP_008986.2:p.Lys1310=
NM_007055.4:c.3930G>A MANE Select	NP_008986.2:p.Lys1310=