Canonical Allele Identifier: CA377335493

Gene: POLR3A

Linked Data

• MyVariant Identifiers: chr10:g.79759782A>G (hg19) ; chr10:g.78000024A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.78000024A>G , CM000672.2:g.78000024A>G	GRCh38
NC_000010.10:g.79759782A>G , CM000672.1:g.79759782A>G	GRCh37
NC_000010.9:g.79429788A>G	NCBI36
NG_029648.1:g.34517T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698727.1:n.1633T>C
ENST00000698728.1:n.2152T>C
ENST00000698729.1:n.3698T>C
ENST00000698730.1:n.3698T>C
ENST00000698731.1:c.2432T>C	ENSP00000513898.1:p.Leu811Pro
ENST00000698732.1:c.*1434T>C	ENSP00000513899.1:n.*1434T>C
ENST00000698733.1:c.*1760T>C	ENSP00000513900.1:n.*1760T>C
ENST00000698734.1:c.2573T>C	ENSP00000513901.1:p.Leu858Pro
ENST00000698735.1:n.2688T>C
ENST00000698736.1:n.2688T>C
ENST00000698737.1:n.2688T>C
ENST00000698738.1:n.2688T>C
ENST00000698739.1:n.2688T>C
ENST00000372371.8:c.2573T>C MANE Select	ENSP00000361446.3:p.Leu858Pro
ENST00000372371.7:c.2573T>C	ENSP00000361446.3:p.Leu858Pro
ENST00000472014.5:n.469+4692T>C
NM_007055.3:c.2573T>C	NP_008986.2:p.Leu858Pro
NM_007055.4:c.2573T>C MANE Select	NP_008986.2:p.Leu858Pro