Canonical Allele Identifier: CA377326057

Gene: POLR3A

Linked Data

• MyVariant Identifiers: chr10:g.79739958T>G (hg19) ; chr10:g.77980200T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.77980200T>G , CM000672.2:g.77980200T>G	GRCh38
NC_000010.10:g.79739958T>G , CM000672.1:g.79739958T>G	GRCh37
NC_000010.9:g.79409964T>G	NCBI36
NG_029648.1:g.54341A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698724.1:n.1882A>C
ENST00000698725.1:n.1635A>C
ENST00000698726.1:n.3195A>C
ENST00000698727.1:n.2928A>C
ENST00000698728.1:n.3544A>C
ENST00000698729.1:n.4992A>C
ENST00000698730.1:n.5090A>C
ENST00000698731.1:c.3824A>C	ENSP00000513898.1:p.Glu1275Ala
ENST00000698732.1:c.*2654A>C	ENSP00000513899.1:n.*2654A>C
ENST00000698733.1:c.*3152A>C	ENSP00000513900.1:n.*3152A>C
ENST00000698734.1:c.*2138A>C	ENSP00000513901.1:n.*2138A>C
ENST00000698735.1:n.4316A>C
ENST00000698736.1:n.4729A>C
ENST00000698737.1:n.4080A>C
ENST00000372371.8:c.3965A>C MANE Select	ENSP00000361446.3:p.Glu1322Ala
ENST00000372371.7:c.3965A>C	ENSP00000361446.3:p.Glu1322Ala
ENST00000616246.4:c.413A>C	ENSP00000483738.1:p.Glu138Ala
NM_007055.3:c.3965A>C	NP_008986.2:p.Glu1322Ala
NM_007055.4:c.3965A>C MANE Select	NP_008986.2:p.Glu1322Ala