Canonical Allele Identifier: CA377326084

Gene: POLR3A

Linked Data

• MyVariant Identifiers: chr10:g.79739971G>C (hg19) ; chr10:g.77980213G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.77980213G>C , CM000672.2:g.77980213G>C	GRCh38
NC_000010.10:g.79739971G>C , CM000672.1:g.79739971G>C	GRCh37
NC_000010.9:g.79409977G>C	NCBI36
NG_029648.1:g.54328C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698724.1:n.1869C>G
ENST00000698725.1:n.1622C>G
ENST00000698726.1:n.3182C>G
ENST00000698727.1:n.2915C>G
ENST00000698728.1:n.3531C>G
ENST00000698729.1:n.4979C>G
ENST00000698730.1:n.5077C>G
ENST00000698731.1:c.3811C>G	ENSP00000513898.1:p.Leu1271Val
ENST00000698732.1:c.*2641C>G	ENSP00000513899.1:n.*2641C>G
ENST00000698733.1:c.*3139C>G	ENSP00000513900.1:n.*3139C>G
ENST00000698734.1:c.*2125C>G	ENSP00000513901.1:n.*2125C>G
ENST00000698735.1:n.4303C>G
ENST00000698736.1:n.4716C>G
ENST00000698737.1:n.4067C>G
ENST00000372371.8:c.3952C>G MANE Select	ENSP00000361446.3:p.Leu1318Val
ENST00000372371.7:c.3952C>G	ENSP00000361446.3:p.Leu1318Val
ENST00000616246.4:c.400C>G	ENSP00000483738.1:p.Leu134Val
NM_007055.3:c.3952C>G	NP_008986.2:p.Leu1318Val
NM_007055.4:c.3952C>G MANE Select	NP_008986.2:p.Leu1318Val