Canonical Allele Identifier: CA470390693

Gene: POLR3A

Linked Data

• MyVariant Identifiers: chr10:g.79740020C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.77980262C>T , CM000672.2:g.77980262C>T	GRCh38
NC_000010.10:g.79740020C>T , CM000672.1:g.79740020C>T	GRCh37
NC_000010.9:g.79410026C>T	NCBI36
NG_029648.1:g.54279G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698724.1:n.1820G>A
ENST00000698725.1:n.1573G>A
ENST00000698726.1:n.3133G>A
ENST00000698727.1:n.2866G>A
ENST00000698728.1:n.3482G>A
ENST00000698729.1:n.4930G>A
ENST00000698730.1:n.5028G>A
ENST00000698731.1:c.3762G>A	ENSP00000513898.1:p.Leu1254=
ENST00000698732.1:c.*2592G>A	ENSP00000513899.1:n.*2592G>A
ENST00000698733.1:c.*3090G>A	ENSP00000513900.1:n.*3090G>A
ENST00000698734.1:c.*2076G>A	ENSP00000513901.1:n.*2076G>A
ENST00000698735.1:n.4254G>A
ENST00000698736.1:n.4667G>A
ENST00000698737.1:n.4018G>A
ENST00000372371.8:c.3903G>A MANE Select	ENSP00000361446.3:p.Leu1301=
ENST00000372371.7:c.3903G>A	ENSP00000361446.3:p.Leu1301=
ENST00000616246.4:c.351G>A	ENSP00000483738.1:p.Leu117=
NM_007055.3:c.3903G>A	NP_008986.2:p.Leu1301=
NM_007055.4:c.3903G>A MANE Select	NP_008986.2:p.Leu1301=