Canonical Allele Identifier: CA470390627

Gene: POLR3A

Linked Data

• MyVariant Identifiers: chr10:g.79739918C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.77980160C>A , CM000672.2:g.77980160C>A	GRCh38
NC_000010.10:g.79739918C>A , CM000672.1:g.79739918C>A	GRCh37
NC_000010.9:g.79409924C>A	NCBI36
NG_029648.1:g.54381G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698724.1:n.1922G>T
ENST00000698725.1:n.1675G>T
ENST00000698726.1:n.3235G>T
ENST00000698727.1:n.2968G>T
ENST00000698728.1:n.3584G>T
ENST00000698729.1:n.5032G>T
ENST00000698730.1:n.5130G>T
ENST00000698731.1:c.3864G>T	ENSP00000513898.1:p.Gly1288=
ENST00000698732.1:c.*2694G>T	ENSP00000513899.1:n.*2694G>T
ENST00000698733.1:c.*3192G>T	ENSP00000513900.1:n.*3192G>T
ENST00000698734.1:c.*2178G>T	ENSP00000513901.1:n.*2178G>T
ENST00000698735.1:n.4356G>T
ENST00000698736.1:n.4769G>T
ENST00000698737.1:n.4120G>T
ENST00000372371.8:c.4005G>T MANE Select	ENSP00000361446.3:p.Gly1335=
ENST00000372371.7:c.4005G>T	ENSP00000361446.3:p.Gly1335=
ENST00000616246.4:c.453G>T	ENSP00000483738.1:p.Gly151=
NM_007055.3:c.4005G>T	NP_008986.2:p.Gly1335=
NM_007055.4:c.4005G>T MANE Select	NP_008986.2:p.Gly1335=