Canonical Allele Identifier: CA377336989

Gene: POLR3A

Linked Data

• COSMIC: COSM4016180
• MyVariant Identifiers: chr10:g.79761991T>C (hg19) ; chr10:g.78002233T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.78002233T>C , CM000672.2:g.78002233T>C	GRCh38
NC_000010.10:g.79761991T>C , CM000672.1:g.79761991T>C	GRCh37
NC_000010.9:g.79431997T>C	NCBI36
NG_029648.1:g.32308A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698727.1:n.1383A>G
ENST00000698728.1:n.1902A>G
ENST00000698729.1:n.3448A>G
ENST00000698730.1:n.3448A>G
ENST00000698731.1:c.2182A>G	ENSP00000513898.1:p.Asn728Asp
ENST00000698732.1:c.*1184A>G	ENSP00000513899.1:n.*1184A>G
ENST00000698733.1:c.*1510A>G	ENSP00000513900.1:n.*1510A>G
ENST00000698734.1:c.2323A>G	ENSP00000513901.1:p.Asn775Asp
ENST00000698735.1:n.2438A>G
ENST00000698736.1:n.2438A>G
ENST00000698737.1:n.2438A>G
ENST00000698738.1:n.2438A>G
ENST00000698739.1:n.2438A>G
ENST00000372371.8:c.2323A>G MANE Select	ENSP00000361446.3:p.Asn775Asp
ENST00000372371.7:c.2323A>G	ENSP00000361446.3:p.Asn775Asp
ENST00000472014.5:n.469+2483A>G
ENST00000473588.2:c.986A>G
NM_007055.3:c.2323A>G	NP_008986.2:p.Asn775Asp
NM_007055.4:c.2323A>G MANE Select	NP_008986.2:p.Asn775Asp