Canonical Allele Identifier: CA377326107
Gene: POLR3A HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000698724.1:n.1859T>A
ENST00000698725.1:n.1612T>A
ENST00000698726.1:n.3172T>A
ENST00000698727.1:n.2905T>A
ENST00000698728.1:n.3521T>A
ENST00000698729.1:n.4969T>A
ENST00000698730.1:n.5067T>A
ENST00000698731.1:c.3801T>A ENSP00000513898.1:p.Ser1267Arg
ENST00000698732.1:c.*2631T>A ENSP00000513899.1:n.*2631T>A
ENST00000698733.1:c.*3129T>A ENSP00000513900.1:n.*3129T>A
ENST00000698734.1:c.*2115T>A ENSP00000513901.1:n.*2115T>A
ENST00000698735.1:n.4293T>A
ENST00000698736.1:n.4706T>A
ENST00000698737.1:n.4057T>A
ENST00000372371.8:c.3942T>A MANE Select ENSP00000361446.3:p.Ser1314Arg
ENST00000372371.7:c.3942T>A ENSP00000361446.3:p.Ser1314Arg
ENST00000616246.4:c.390T>A ENSP00000483738.1:p.Ser130Arg
NM_007055.3:c.3942T>A NP_008986.2:p.Ser1314Arg
NM_007055.4:c.3942T>A MANE Select NP_008986.2:p.Ser1314Arg