Canonical Allele Identifier: CA377326149

Gene: POLR3A

Linked Data

• MyVariant Identifiers: chr10:g.79739998C>G (hg19) ; chr10:g.77980240C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.77980240C>G , CM000672.2:g.77980240C>G	GRCh38
NC_000010.10:g.79739998C>G , CM000672.1:g.79739998C>G	GRCh37
NC_000010.9:g.79410004C>G	NCBI36
NG_029648.1:g.54301G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698724.1:n.1842G>C
ENST00000698725.1:n.1595G>C
ENST00000698726.1:n.3155G>C
ENST00000698727.1:n.2888G>C
ENST00000698728.1:n.3504G>C
ENST00000698729.1:n.4952G>C
ENST00000698730.1:n.5050G>C
ENST00000698731.1:c.3784G>C	ENSP00000513898.1:p.Ala1262Pro
ENST00000698732.1:c.*2614G>C	ENSP00000513899.1:n.*2614G>C
ENST00000698733.1:c.*3112G>C	ENSP00000513900.1:n.*3112G>C
ENST00000698734.1:c.*2098G>C	ENSP00000513901.1:n.*2098G>C
ENST00000698735.1:n.4276G>C
ENST00000698736.1:n.4689G>C
ENST00000698737.1:n.4040G>C
ENST00000372371.8:c.3925G>C MANE Select	ENSP00000361446.3:p.Ala1309Pro
ENST00000372371.7:c.3925G>C	ENSP00000361446.3:p.Ala1309Pro
ENST00000616246.4:c.373G>C	ENSP00000483738.1:p.Ala125Pro
NM_007055.3:c.3925G>C	NP_008986.2:p.Ala1309Pro
NM_007055.4:c.3925G>C MANE Select	NP_008986.2:p.Ala1309Pro