Canonical Allele Identifier: CA1921497564

Gene: POLR3A

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.77980315T= , CM000672.2:g.77980315T=	GRCh38
NC_000010.10:g.79740073T= , CM000672.1:g.79740073T=	GRCh37
NC_000010.9:g.79410079T=	NCBI36
NG_029648.1:g.54226A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698724.1:n.1809-42A=
ENST00000698725.1:n.1520A=
ENST00000698726.1:n.3122-42A=
ENST00000698727.1:n.2855-42A=
ENST00000698728.1:n.3471-42A=
ENST00000698729.1:n.4919-42A=
ENST00000698730.1:n.5017-42A=
ENST00000698731.1:c.3751-42A=	ENSP00000513898.1:n.3751-42A=
ENST00000698732.1:c.*2581-42A=	ENSP00000513899.1:n.*2581-42A=
ENST00000698733.1:c.*3079-42A=	ENSP00000513900.1:n.*3079-42A=
ENST00000698734.1:c.*2065-42A=	ENSP00000513901.1:n.*2065-42A=
ENST00000698735.1:n.4243-42A=
ENST00000698736.1:n.4656-42A=
ENST00000698737.1:n.4007-42A=
ENST00000372371.8:c.3892-42A= MANE Select	ENSP00000361446.3:n.3892-42A=
ENST00000372371.7:c.3892-42A=	ENSP00000361446.3:n.3892-42A=
ENST00000616246.4:c.340-42A=	ENSP00000483738.1:n.340-42A=
NM_007055.3:c.3892-42A=	NP_008986.2:n.3892-42A=
NM_007055.4:c.3892-42A= MANE Select	NP_008986.2:n.3892-42A=