Canonical Allele Identifier: CA470390667

Gene: POLR3A

Linked Data

• MyVariant Identifiers: chr10:g.79739981A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.77980223A>G , CM000672.2:g.77980223A>G	GRCh38
NC_000010.10:g.79739981A>G , CM000672.1:g.79739981A>G	GRCh37
NC_000010.9:g.79409987A>G	NCBI36
NG_029648.1:g.54318T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698724.1:n.1859T>C
ENST00000698725.1:n.1612T>C
ENST00000698726.1:n.3172T>C
ENST00000698727.1:n.2905T>C
ENST00000698728.1:n.3521T>C
ENST00000698729.1:n.4969T>C
ENST00000698730.1:n.5067T>C
ENST00000698731.1:c.3801T>C	ENSP00000513898.1:p.Ser1267=
ENST00000698732.1:c.*2631T>C	ENSP00000513899.1:n.*2631T>C
ENST00000698733.1:c.*3129T>C	ENSP00000513900.1:n.*3129T>C
ENST00000698734.1:c.*2115T>C	ENSP00000513901.1:n.*2115T>C
ENST00000698735.1:n.4293T>C
ENST00000698736.1:n.4706T>C
ENST00000698737.1:n.4057T>C
ENST00000372371.8:c.3942T>C MANE Select	ENSP00000361446.3:p.Ser1314=
ENST00000372371.7:c.3942T>C	ENSP00000361446.3:p.Ser1314=
ENST00000616246.4:c.390T>C	ENSP00000483738.1:p.Ser130=
NM_007055.3:c.3942T>C	NP_008986.2:p.Ser1314=
NM_007055.4:c.3942T>C MANE Select	NP_008986.2:p.Ser1314=