Canonical Allele Identifier: CA377325934

Gene: POLR3A

Linked Data

• MyVariant Identifiers: chr10:g.79739904A>G (hg19) ; chr10:g.77980146A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.77980146A>G , CM000672.2:g.77980146A>G	GRCh38
NC_000010.10:g.79739904A>G , CM000672.1:g.79739904A>G	GRCh37
NC_000010.9:g.79409910A>G	NCBI36
NG_029648.1:g.54395T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698724.1:n.1936T>C
ENST00000698725.1:n.1689T>C
ENST00000698726.1:n.3249T>C
ENST00000698727.1:n.2982T>C
ENST00000698728.1:n.3598T>C
ENST00000698729.1:n.5046T>C
ENST00000698730.1:n.5144T>C
ENST00000698731.1:c.3878T>C	ENSP00000513898.1:p.Val1293Ala
ENST00000698732.1:c.*2708T>C	ENSP00000513899.1:n.*2708T>C
ENST00000698733.1:c.*3206T>C	ENSP00000513900.1:n.*3206T>C
ENST00000698734.1:c.*2192T>C	ENSP00000513901.1:n.*2192T>C
ENST00000698735.1:n.4370T>C
ENST00000698736.1:n.4783T>C
ENST00000698737.1:n.4134T>C
ENST00000372371.8:c.4019T>C MANE Select	ENSP00000361446.3:p.Val1340Ala
ENST00000372371.7:c.4019T>C	ENSP00000361446.3:p.Val1340Ala
ENST00000616246.4:c.467T>C	ENSP00000483738.1:p.Val156Ala
NM_007055.3:c.4019T>C	NP_008986.2:p.Val1340Ala
NM_007055.4:c.4019T>C MANE Select	NP_008986.2:p.Val1340Ala