Canonical Allele Identifier: CA377334023

Gene: POLR3A

Linked Data

• MyVariant Identifiers: chr10:g.79752995T>G (hg19) ; chr10:g.77993237T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.77993237T>G , CM000672.2:g.77993237T>G	GRCh38
NC_000010.10:g.79752995T>G , CM000672.1:g.79752995T>G	GRCh37
NC_000010.9:g.79423001T>G	NCBI36
NG_029648.1:g.41304A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000698724.1:n.15A>C
ENST00000698727.1:n.1807A>C
ENST00000698728.1:n.2326A>C
ENST00000698729.1:n.3872A>C
ENST00000698730.1:n.3872A>C
ENST00000698731.1:c.2606A>C	ENSP00000513898.1:p.Asp869Ala
ENST00000698732.1:c.*1608A>C	ENSP00000513899.1:n.*1608A>C
ENST00000698733.1:c.*1934A>C	ENSP00000513900.1:n.*1934A>C
ENST00000698734.1:c.*271A>C	ENSP00000513901.1:n.*271A>C
ENST00000698735.1:n.2862A>C
ENST00000698736.1:n.2862A>C
ENST00000698737.1:n.2862A>C
ENST00000698738.1:n.2862A>C
ENST00000698739.1:n.2862A>C
ENST00000372371.8:c.2747A>C MANE Select	ENSP00000361446.3:p.Asp916Ala
ENST00000372371.7:c.2747A>C	ENSP00000361446.3:p.Asp916Ala
ENST00000472014.5:n.600A>C
NM_007055.3:c.2747A>C	NP_008986.2:p.Asp916Ala
NM_007055.4:c.2747A>C MANE Select	NP_008986.2:p.Asp916Ala