Canonical Allele Identifier: CA470390698

Gene: POLR3A

Linked Data

• MyVariant Identifiers: chr10:g.79740029A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.77980271A>C , CM000672.2:g.77980271A>C	GRCh38
NC_000010.10:g.79740029A>C , CM000672.1:g.79740029A>C	GRCh37
NC_000010.9:g.79410035A>C	NCBI36
NG_029648.1:g.54270T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698724.1:n.1811T>G
ENST00000698725.1:n.1564T>G
ENST00000698726.1:n.3124T>G
ENST00000698727.1:n.2857T>G
ENST00000698728.1:n.3473T>G
ENST00000698729.1:n.4921T>G
ENST00000698730.1:n.5019T>G
ENST00000698731.1:c.3753T>G	ENSP00000513898.1:p.Gly1251=
ENST00000698732.1:c.*2583T>G	ENSP00000513899.1:n.*2583T>G
ENST00000698733.1:c.*3081T>G	ENSP00000513900.1:n.*3081T>G
ENST00000698734.1:c.*2067T>G	ENSP00000513901.1:n.*2067T>G
ENST00000698735.1:n.4245T>G
ENST00000698736.1:n.4658T>G
ENST00000698737.1:n.4009T>G
ENST00000372371.8:c.3894T>G MANE Select	ENSP00000361446.3:p.Gly1298=
ENST00000372371.7:c.3894T>G	ENSP00000361446.3:p.Gly1298=
ENST00000616246.4:c.342T>G	ENSP00000483738.1:p.Gly114=
NM_007055.3:c.3894T>G	NP_008986.2:p.Gly1298=
NM_007055.4:c.3894T>G MANE Select	NP_008986.2:p.Gly1298=