Canonical Allele Identifier: CA377335794

Gene: POLR3A

Linked Data

• MyVariant Identifiers: chr10:g.79759864T>G (hg19) ; chr10:g.78000106T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.78000106T>G , CM000672.2:g.78000106T>G	GRCh38
NC_000010.10:g.79759864T>G , CM000672.1:g.79759864T>G	GRCh37
NC_000010.9:g.79429870T>G	NCBI36
NG_029648.1:g.34435A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698727.1:n.1551A>C
ENST00000698728.1:n.2070A>C
ENST00000698729.1:n.3616A>C
ENST00000698730.1:n.3616A>C
ENST00000698731.1:c.2350A>C	ENSP00000513898.1:p.Lys784Gln
ENST00000698732.1:c.*1352A>C	ENSP00000513899.1:n.*1352A>C
ENST00000698733.1:c.*1678A>C	ENSP00000513900.1:n.*1678A>C
ENST00000698734.1:c.2491A>C	ENSP00000513901.1:p.Lys831Gln
ENST00000698735.1:n.2606A>C
ENST00000698736.1:n.2606A>C
ENST00000698737.1:n.2606A>C
ENST00000698738.1:n.2606A>C
ENST00000698739.1:n.2606A>C
ENST00000372371.8:c.2491A>C MANE Select	ENSP00000361446.3:p.Lys831Gln
ENST00000372371.7:c.2491A>C	ENSP00000361446.3:p.Lys831Gln
ENST00000472014.5:n.469+4610A>C
NM_007055.3:c.2491A>C	NP_008986.2:p.Lys831Gln
NM_007055.4:c.2491A>C MANE Select	NP_008986.2:p.Lys831Gln