Canonical Allele Identifier: CA377326185

Gene: POLR3A

Linked Data

• MyVariant Identifiers: chr10:g.79740015A>G (hg19) ; chr10:g.77980257A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.77980257A>G , CM000672.2:g.77980257A>G	GRCh38
NC_000010.10:g.79740015A>G , CM000672.1:g.79740015A>G	GRCh37
NC_000010.9:g.79410021A>G	NCBI36
NG_029648.1:g.54284T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698724.1:n.1825T>C
ENST00000698725.1:n.1578T>C
ENST00000698726.1:n.3138T>C
ENST00000698727.1:n.2871T>C
ENST00000698728.1:n.3487T>C
ENST00000698729.1:n.4935T>C
ENST00000698730.1:n.5033T>C
ENST00000698731.1:c.3767T>C	ENSP00000513898.1:p.Ile1256Thr
ENST00000698732.1:c.*2597T>C	ENSP00000513899.1:n.*2597T>C
ENST00000698733.1:c.*3095T>C	ENSP00000513900.1:n.*3095T>C
ENST00000698734.1:c.*2081T>C	ENSP00000513901.1:n.*2081T>C
ENST00000698735.1:n.4259T>C
ENST00000698736.1:n.4672T>C
ENST00000698737.1:n.4023T>C
ENST00000372371.8:c.3908T>C MANE Select	ENSP00000361446.3:p.Ile1303Thr
ENST00000372371.7:c.3908T>C	ENSP00000361446.3:p.Ile1303Thr
ENST00000616246.4:c.356T>C	ENSP00000483738.1:p.Ile119Thr
NM_007055.3:c.3908T>C	NP_008986.2:p.Ile1303Thr
NM_007055.4:c.3908T>C MANE Select	NP_008986.2:p.Ile1303Thr