Canonical Allele Identifier: CA377326181

Gene: POLR3A

Linked Data

• MyVariant Identifiers: chr10:g.79740013T>G (hg19) ; chr10:g.77980255T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.77980255T>G , CM000672.2:g.77980255T>G	GRCh38
NC_000010.10:g.79740013T>G , CM000672.1:g.79740013T>G	GRCh37
NC_000010.9:g.79410019T>G	NCBI36
NG_029648.1:g.54286A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698724.1:n.1827A>C
ENST00000698725.1:n.1580A>C
ENST00000698726.1:n.3140A>C
ENST00000698727.1:n.2873A>C
ENST00000698728.1:n.3489A>C
ENST00000698729.1:n.4937A>C
ENST00000698730.1:n.5035A>C
ENST00000698731.1:c.3769A>C	ENSP00000513898.1:p.Thr1257Pro
ENST00000698732.1:c.*2599A>C	ENSP00000513899.1:n.*2599A>C
ENST00000698733.1:c.*3097A>C	ENSP00000513900.1:n.*3097A>C
ENST00000698734.1:c.*2083A>C	ENSP00000513901.1:n.*2083A>C
ENST00000698735.1:n.4261A>C
ENST00000698736.1:n.4674A>C
ENST00000698737.1:n.4025A>C
ENST00000372371.8:c.3910A>C MANE Select	ENSP00000361446.3:p.Thr1304Pro
ENST00000372371.7:c.3910A>C	ENSP00000361446.3:p.Thr1304Pro
ENST00000616246.4:c.358A>C	ENSP00000483738.1:p.Thr120Pro
NM_007055.3:c.3910A>C	NP_008986.2:p.Thr1304Pro
NM_007055.4:c.3910A>C MANE Select	NP_008986.2:p.Thr1304Pro