Canonical Allele Identifier: CA1921497594

Gene: POLR3A

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.77980373C= , CM000672.2:g.77980373C=	GRCh38
NC_000010.10:g.79740131C= , CM000672.1:g.79740131C=	GRCh37
NC_000010.9:g.79410137C=	NCBI36
NG_029648.1:g.54168G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698724.1:n.1809-100G=
ENST00000698725.1:n.1462G=
ENST00000698726.1:n.3122-100G=
ENST00000698727.1:n.2855-100G=
ENST00000698728.1:n.3471-100G=
ENST00000698729.1:n.4919-100G=
ENST00000698730.1:n.5017-100G=
ENST00000698731.1:c.3751-100G=	ENSP00000513898.1:n.3751-100G=
ENST00000698732.1:c.*2581-100G=	ENSP00000513899.1:n.*2581-100G=
ENST00000698733.1:c.*3079-100G=	ENSP00000513900.1:n.*3079-100G=
ENST00000698734.1:c.*2065-100G=	ENSP00000513901.1:n.*2065-100G=
ENST00000698735.1:n.4243-100G=
ENST00000698736.1:n.4656-100G=
ENST00000698737.1:n.4007-100G=
ENST00000372371.8:c.3892-100G= MANE Select	ENSP00000361446.3:n.3892-100G=
ENST00000372371.7:c.3892-100G=	ENSP00000361446.3:n.3892-100G=
ENST00000616246.4:c.340-100G=	ENSP00000483738.1:n.340-100G=
NM_007055.3:c.3892-100G=	NP_008986.2:n.3892-100G=
NM_007055.4:c.3892-100G= MANE Select	NP_008986.2:n.3892-100G=