Canonical Allele Identifier: CA1921497580

Gene: POLR3A

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.77980352A= , CM000672.2:g.77980352A=	GRCh38
NC_000010.10:g.79740110A= , CM000672.1:g.79740110A=	GRCh37
NC_000010.9:g.79410116A=	NCBI36
NG_029648.1:g.54189T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698724.1:n.1809-79T=
ENST00000698725.1:n.1483T=
ENST00000698726.1:n.3122-79T=
ENST00000698727.1:n.2855-79T=
ENST00000698728.1:n.3471-79T=
ENST00000698729.1:n.4919-79T=
ENST00000698730.1:n.5017-79T=
ENST00000698731.1:c.3751-79T=	ENSP00000513898.1:n.3751-79T=
ENST00000698732.1:c.*2581-79T=	ENSP00000513899.1:n.*2581-79T=
ENST00000698733.1:c.*3079-79T=	ENSP00000513900.1:n.*3079-79T=
ENST00000698734.1:c.*2065-79T=	ENSP00000513901.1:n.*2065-79T=
ENST00000698735.1:n.4243-79T=
ENST00000698736.1:n.4656-79T=
ENST00000698737.1:n.4007-79T=
ENST00000372371.8:c.3892-79T= MANE Select	ENSP00000361446.3:n.3892-79T=
ENST00000372371.7:c.3892-79T=	ENSP00000361446.3:n.3892-79T=
ENST00000616246.4:c.340-79T=	ENSP00000483738.1:n.340-79T=
NM_007055.3:c.3892-79T=	NP_008986.2:n.3892-79T=
NM_007055.4:c.3892-79T= MANE Select	NP_008986.2:n.3892-79T=