Canonical Allele Identifier: CA377326119

Gene: POLR3A

Linked Data

• dbSNP Id: rs1469103073
• MyVariant Identifiers: chr10:g.79739986C>G (hg19) ; chr10:g.77980228C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.77980228C>G , CM000672.2:g.77980228C>G	GRCh38
NC_000010.10:g.79739986C>G , CM000672.1:g.79739986C>G	GRCh37
NC_000010.9:g.79409992C>G	NCBI36
NG_029648.1:g.54313G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698724.1:n.1854G>C
ENST00000698725.1:n.1607G>C
ENST00000698726.1:n.3167G>C
ENST00000698727.1:n.2900G>C
ENST00000698728.1:n.3516G>C
ENST00000698729.1:n.4964G>C
ENST00000698730.1:n.5062G>C
ENST00000698731.1:c.3796G>C	ENSP00000513898.1:p.Glu1266Gln
ENST00000698732.1:c.*2626G>C	ENSP00000513899.1:n.*2626G>C
ENST00000698733.1:c.*3124G>C	ENSP00000513900.1:n.*3124G>C
ENST00000698734.1:c.*2110G>C	ENSP00000513901.1:n.*2110G>C
ENST00000698735.1:n.4288G>C
ENST00000698736.1:n.4701G>C
ENST00000698737.1:n.4052G>C
ENST00000372371.8:c.3937G>C MANE Select	ENSP00000361446.3:p.Glu1313Gln
ENST00000372371.7:c.3937G>C	ENSP00000361446.3:p.Glu1313Gln
ENST00000616246.4:c.385G>C	ENSP00000483738.1:p.Glu129Gln
NM_007055.3:c.3937G>C	NP_008986.2:p.Glu1313Gln
NM_007055.4:c.3937G>C MANE Select	NP_008986.2:p.Glu1313Gln