Canonical Allele Identifier: CA470390645

Gene: POLR3A

Linked Data

• MyVariant Identifiers: chr10:g.79739948A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.77980190A>T , CM000672.2:g.77980190A>T	GRCh38
NC_000010.10:g.79739948A>T , CM000672.1:g.79739948A>T	GRCh37
NC_000010.9:g.79409954A>T	NCBI36
NG_029648.1:g.54351T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698724.1:n.1892T>A
ENST00000698725.1:n.1645T>A
ENST00000698726.1:n.3205T>A
ENST00000698727.1:n.2938T>A
ENST00000698728.1:n.3554T>A
ENST00000698729.1:n.5002T>A
ENST00000698730.1:n.5100T>A
ENST00000698731.1:c.3834T>A	ENSP00000513898.1:p.Ala1278=
ENST00000698732.1:c.*2664T>A	ENSP00000513899.1:n.*2664T>A
ENST00000698733.1:c.*3162T>A	ENSP00000513900.1:n.*3162T>A
ENST00000698734.1:c.*2148T>A	ENSP00000513901.1:n.*2148T>A
ENST00000698735.1:n.4326T>A
ENST00000698736.1:n.4739T>A
ENST00000698737.1:n.4090T>A
ENST00000372371.8:c.3975T>A MANE Select	ENSP00000361446.3:p.Ala1325=
ENST00000372371.7:c.3975T>A	ENSP00000361446.3:p.Ala1325=
ENST00000616246.4:c.423T>A	ENSP00000483738.1:p.Ala141=
NM_007055.3:c.3975T>A	NP_008986.2:p.Ala1325=
NM_007055.4:c.3975T>A MANE Select	NP_008986.2:p.Ala1325=