Canonical Allele Identifier: CA470390621

Gene: POLR3A

Linked Data

• MyVariant Identifiers: chr10:g.79739906A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.77980148A>T , CM000672.2:g.77980148A>T	GRCh38
NC_000010.10:g.79739906A>T , CM000672.1:g.79739906A>T	GRCh37
NC_000010.9:g.79409912A>T	NCBI36
NG_029648.1:g.54393T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698724.1:n.1934T>A
ENST00000698725.1:n.1687T>A
ENST00000698726.1:n.3247T>A
ENST00000698727.1:n.2980T>A
ENST00000698728.1:n.3596T>A
ENST00000698729.1:n.5044T>A
ENST00000698730.1:n.5142T>A
ENST00000698731.1:c.3876T>A	ENSP00000513898.1:p.Ser1292=
ENST00000698732.1:c.*2706T>A	ENSP00000513899.1:n.*2706T>A
ENST00000698733.1:c.*3204T>A	ENSP00000513900.1:n.*3204T>A
ENST00000698734.1:c.*2190T>A	ENSP00000513901.1:n.*2190T>A
ENST00000698735.1:n.4368T>A
ENST00000698736.1:n.4781T>A
ENST00000698737.1:n.4132T>A
ENST00000372371.8:c.4017T>A MANE Select	ENSP00000361446.3:p.Ser1339=
ENST00000372371.7:c.4017T>A	ENSP00000361446.3:p.Ser1339=
ENST00000616246.4:c.465T>A	ENSP00000483738.1:p.Ser155=
NM_007055.3:c.4017T>A	NP_008986.2:p.Ser1339=
NM_007055.4:c.4017T>A MANE Select	NP_008986.2:p.Ser1339=