Canonical Allele Identifier: CA470397176

Gene: POLR3A

Linked Data

• MyVariant Identifiers: chr10:g.79759817C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.78000059C>T , CM000672.2:g.78000059C>T	GRCh38
NC_000010.10:g.79759817C>T , CM000672.1:g.79759817C>T	GRCh37
NC_000010.9:g.79429823C>T	NCBI36
NG_029648.1:g.34482G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698727.1:n.1598G>A
ENST00000698728.1:n.2117G>A
ENST00000698729.1:n.3663G>A
ENST00000698730.1:n.3663G>A
ENST00000698731.1:c.2397G>A	ENSP00000513898.1:p.Glu799=
ENST00000698732.1:c.*1399G>A	ENSP00000513899.1:n.*1399G>A
ENST00000698733.1:c.*1725G>A	ENSP00000513900.1:n.*1725G>A
ENST00000698734.1:c.2538G>A	ENSP00000513901.1:p.Glu846=
ENST00000698735.1:n.2653G>A
ENST00000698736.1:n.2653G>A
ENST00000698737.1:n.2653G>A
ENST00000698738.1:n.2653G>A
ENST00000698739.1:n.2653G>A
ENST00000372371.8:c.2538G>A MANE Select	ENSP00000361446.3:p.Glu846=
ENST00000372371.7:c.2538G>A	ENSP00000361446.3:p.Glu846=
ENST00000472014.5:n.469+4657G>A
NM_007055.3:c.2538G>A	NP_008986.2:p.Glu846=
NM_007055.4:c.2538G>A MANE Select	NP_008986.2:p.Glu846=