Canonical Allele Identifier: CA377340942

Gene: POLR3A

Linked Data

• COSMIC: COSM4016184
• MyVariant Identifiers: chr10:g.79769644A>C (hg19) ; chr10:g.78009886A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.78009886A>C , CM000672.2:g.78009886A>C	GRCh38
NC_000010.10:g.79769644A>C , CM000672.1:g.79769644A>C	GRCh37
NC_000010.9:g.79439650A>C	NCBI36
NG_029648.1:g.24655T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000698728.1:n.1327T>G
ENST00000698729.1:n.2873T>G
ENST00000698730.1:n.2873T>G
ENST00000698731.1:c.1607T>G	ENSP00000513898.1:p.Leu536Arg
ENST00000698732.1:c.*609T>G	ENSP00000513899.1:n.*609T>G
ENST00000698733.1:c.*935T>G	ENSP00000513900.1:n.*935T>G
ENST00000698734.1:c.1748T>G	ENSP00000513901.1:p.Leu583Arg
ENST00000698735.1:n.1863T>G
ENST00000698736.1:n.1863T>G
ENST00000698737.1:n.1863T>G
ENST00000698738.1:n.1863T>G
ENST00000698739.1:n.1863T>G
ENST00000372371.8:c.1748T>G MANE Select	ENSP00000361446.3:p.Leu583Arg
ENST00000372371.7:c.1748T>G	ENSP00000361446.3:p.Leu583Arg
ENST00000473588.2:c.550T>G
NM_007055.3:c.1748T>G	NP_008986.2:p.Leu583Arg
NM_007055.4:c.1748T>G MANE Select	NP_008986.2:p.Leu583Arg