Canonical Allele Identifier: CA377326203

Gene: POLR3A

Linked Data

• MyVariant Identifiers: chr10:g.79740022G>T (hg19) ; chr10:g.77980264G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.77980264G>T , CM000672.2:g.77980264G>T	GRCh38
NC_000010.10:g.79740022G>T , CM000672.1:g.79740022G>T	GRCh37
NC_000010.9:g.79410028G>T	NCBI36
NG_029648.1:g.54277C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698724.1:n.1818C>A
ENST00000698725.1:n.1571C>A
ENST00000698726.1:n.3131C>A
ENST00000698727.1:n.2864C>A
ENST00000698728.1:n.3480C>A
ENST00000698729.1:n.4928C>A
ENST00000698730.1:n.5026C>A
ENST00000698731.1:c.3760C>A	ENSP00000513898.1:p.Leu1254Met
ENST00000698732.1:c.*2590C>A	ENSP00000513899.1:n.*2590C>A
ENST00000698733.1:c.*3088C>A	ENSP00000513900.1:n.*3088C>A
ENST00000698734.1:c.*2074C>A	ENSP00000513901.1:n.*2074C>A
ENST00000698735.1:n.4252C>A
ENST00000698736.1:n.4665C>A
ENST00000698737.1:n.4016C>A
ENST00000372371.8:c.3901C>A MANE Select	ENSP00000361446.3:p.Leu1301Met
ENST00000372371.7:c.3901C>A	ENSP00000361446.3:p.Leu1301Met
ENST00000616246.4:c.349C>A	ENSP00000483738.1:p.Leu117Met
NM_007055.3:c.3901C>A	NP_008986.2:p.Leu1301Met
NM_007055.4:c.3901C>A MANE Select	NP_008986.2:p.Leu1301Met