Canonical Allele Identifier: CA1921508754

Gene: POLR3A

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.78004957A= , CM000672.2:g.78004957A=	GRCh38
NC_000010.10:g.79764715A= , CM000672.1:g.79764715A=	GRCh37
NC_000010.9:g.79434721A=	NCBI36
NG_029648.1:g.29584T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698727.1:n.1135-69T=
ENST00000698728.1:n.1654-69T=
ENST00000698729.1:n.3200-69T=
ENST00000698730.1:n.3200-69T=
ENST00000698731.1:c.1934-69T=	ENSP00000513898.1:n.1934-69T=
ENST00000698732.1:c.*936-69T=	ENSP00000513899.1:n.*936-69T=
ENST00000698733.1:c.*1262-69T=	ENSP00000513900.1:n.*1262-69T=
ENST00000698734.1:c.2075-69T=	ENSP00000513901.1:n.2075-69T=
ENST00000698735.1:n.2190-69T=
ENST00000698736.1:n.2190-69T=
ENST00000698737.1:n.2190-69T=
ENST00000698738.1:n.2190-69T=
ENST00000698739.1:n.2190-69T=
ENST00000372371.8:c.2075-69T= MANE Select	ENSP00000361446.3:n.2075-69T=
ENST00000372371.7:c.2075-69T=	ENSP00000361446.3:n.2075-69T=
ENST00000472014.5:n.297-69T=
ENST00000473588.2:c.738-69T=
NM_007055.3:c.2075-69T=	NP_008986.2:n.2075-69T=
NM_007055.4:c.2075-69T= MANE Select	NP_008986.2:n.2075-69T=