Canonical Allele Identifier: CA470397214

Gene: POLR3A

Linked Data

• MyVariant Identifiers: chr10:g.79759853C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.78000095C>G , CM000672.2:g.78000095C>G	GRCh38
NC_000010.10:g.79759853C>G , CM000672.1:g.79759853C>G	GRCh37
NC_000010.9:g.79429859C>G	NCBI36
NG_029648.1:g.34446G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698727.1:n.1562G>C
ENST00000698728.1:n.2081G>C
ENST00000698729.1:n.3627G>C
ENST00000698730.1:n.3627G>C
ENST00000698731.1:c.2361G>C	ENSP00000513898.1:p.Val787=
ENST00000698732.1:c.*1363G>C	ENSP00000513899.1:n.*1363G>C
ENST00000698733.1:c.*1689G>C	ENSP00000513900.1:n.*1689G>C
ENST00000698734.1:c.2502G>C	ENSP00000513901.1:p.Val834=
ENST00000698735.1:n.2617G>C
ENST00000698736.1:n.2617G>C
ENST00000698737.1:n.2617G>C
ENST00000698738.1:n.2617G>C
ENST00000698739.1:n.2617G>C
ENST00000372371.8:c.2502G>C MANE Select	ENSP00000361446.3:p.Val834=
ENST00000372371.7:c.2502G>C	ENSP00000361446.3:p.Val834=
ENST00000472014.5:n.469+4621G>C
NM_007055.3:c.2502G>C	NP_008986.2:p.Val834=
NM_007055.4:c.2502G>C MANE Select	NP_008986.2:p.Val834=