Canonical Allele Identifier: CA470397234

Gene: POLR3A

Linked Data

• MyVariant Identifiers: chr10:g.79759871T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.78000113T>C , CM000672.2:g.78000113T>C	GRCh38
NC_000010.10:g.79759871T>C , CM000672.1:g.79759871T>C	GRCh37
NC_000010.9:g.79429877T>C	NCBI36
NG_029648.1:g.34428A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698727.1:n.1544A>G
ENST00000698728.1:n.2063A>G
ENST00000698729.1:n.3609A>G
ENST00000698730.1:n.3609A>G
ENST00000698731.1:c.2343A>G	ENSP00000513898.1:p.Pro781=
ENST00000698732.1:c.*1345A>G	ENSP00000513899.1:n.*1345A>G
ENST00000698733.1:c.*1671A>G	ENSP00000513900.1:n.*1671A>G
ENST00000698734.1:c.2484A>G	ENSP00000513901.1:p.Pro828=
ENST00000698735.1:n.2599A>G
ENST00000698736.1:n.2599A>G
ENST00000698737.1:n.2599A>G
ENST00000698738.1:n.2599A>G
ENST00000698739.1:n.2599A>G
ENST00000372371.8:c.2484A>G MANE Select	ENSP00000361446.3:p.Pro828=
ENST00000372371.7:c.2484A>G	ENSP00000361446.3:p.Pro828=
ENST00000472014.5:n.469+4603A>G
NM_007055.3:c.2484A>G	NP_008986.2:p.Pro828=
NM_007055.4:c.2484A>G MANE Select	NP_008986.2:p.Pro828=