Canonical Allele Identifier: CA470397716

Gene: POLR3A

Linked Data

• MyVariant Identifiers: chr10:g.79764618A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.78004860A>C , CM000672.2:g.78004860A>C	GRCh38
NC_000010.10:g.79764618A>C , CM000672.1:g.79764618A>C	GRCh37
NC_000010.9:g.79434624A>C	NCBI36
NG_029648.1:g.29681T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698727.1:n.1163T>G
ENST00000698728.1:n.1682T>G
ENST00000698729.1:n.3228T>G
ENST00000698730.1:n.3228T>G
ENST00000698731.1:c.1962T>G	ENSP00000513898.1:p.Gly654=
ENST00000698732.1:c.*964T>G	ENSP00000513899.1:n.*964T>G
ENST00000698733.1:c.*1290T>G	ENSP00000513900.1:n.*1290T>G
ENST00000698734.1:c.2103T>G	ENSP00000513901.1:p.Gly701=
ENST00000698735.1:n.2218T>G
ENST00000698736.1:n.2218T>G
ENST00000698737.1:n.2218T>G
ENST00000698738.1:n.2218T>G
ENST00000698739.1:n.2218T>G
ENST00000372371.8:c.2103T>G MANE Select	ENSP00000361446.3:p.Gly701=
ENST00000372371.7:c.2103T>G	ENSP00000361446.3:p.Gly701=
ENST00000472014.5:n.325T>G
ENST00000473588.2:c.766T>G
NM_007055.3:c.2103T>G	NP_008986.2:p.Gly701=
NM_007055.4:c.2103T>G MANE Select	NP_008986.2:p.Gly701=