Canonical Allele Identifier: CA377326065
Gene: POLR3A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.77980203A>T , CM000672.2:g.77980203A>T GRCh38
NC_000010.10:g.79739961A>T , CM000672.1:g.79739961A>T GRCh37
NC_000010.9:g.79409967A>T NCBI36
NG_029648.1:g.54338T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000698724.1:n.1879T>A
ENST00000698725.1:n.1632T>A
ENST00000698726.1:n.3192T>A
ENST00000698727.1:n.2925T>A
ENST00000698728.1:n.3541T>A
ENST00000698729.1:n.4989T>A
ENST00000698730.1:n.5087T>A
ENST00000698731.1:c.3821T>A ENSP00000513898.1:p.Phe1274Tyr
ENST00000698732.1:c.*2651T>A ENSP00000513899.1:n.*2651T>A
ENST00000698733.1:c.*3149T>A ENSP00000513900.1:n.*3149T>A
ENST00000698734.1:c.*2135T>A ENSP00000513901.1:n.*2135T>A
ENST00000698735.1:n.4313T>A
ENST00000698736.1:n.4726T>A
ENST00000698737.1:n.4077T>A
ENST00000372371.8:c.3962T>A MANE Select ENSP00000361446.3:p.Phe1321Tyr
ENST00000372371.7:c.3962T>A ENSP00000361446.3:p.Phe1321Tyr
ENST00000616246.4:c.410T>A ENSP00000483738.1:p.Phe137Tyr
NM_007055.3:c.3962T>A NP_008986.2:p.Phe1321Tyr
NM_007055.4:c.3962T>A MANE Select NP_008986.2:p.Phe1321Tyr