Canonical Allele Identifier: CA377325976
Gene: POLR3A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.77980165A>G , CM000672.2:g.77980165A>G GRCh38
NC_000010.10:g.79739923A>G , CM000672.1:g.79739923A>G GRCh37
NC_000010.9:g.79409929A>G NCBI36
NG_029648.1:g.54376T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000698724.1:n.1917T>C
ENST00000698725.1:n.1670T>C
ENST00000698726.1:n.3230T>C
ENST00000698727.1:n.2963T>C
ENST00000698728.1:n.3579T>C
ENST00000698729.1:n.5027T>C
ENST00000698730.1:n.5125T>C
ENST00000698731.1:c.3859T>C ENSP00000513898.1:p.Phe1287Leu
ENST00000698732.1:c.*2689T>C ENSP00000513899.1:n.*2689T>C
ENST00000698733.1:c.*3187T>C ENSP00000513900.1:n.*3187T>C
ENST00000698734.1:c.*2173T>C ENSP00000513901.1:n.*2173T>C
ENST00000698735.1:n.4351T>C
ENST00000698736.1:n.4764T>C
ENST00000698737.1:n.4115T>C
ENST00000372371.8:c.4000T>C MANE Select ENSP00000361446.3:p.Phe1334Leu
ENST00000372371.7:c.4000T>C ENSP00000361446.3:p.Phe1334Leu
ENST00000616246.4:c.448T>C ENSP00000483738.1:p.Phe150Leu
NM_007055.3:c.4000T>C NP_008986.2:p.Phe1334Leu
NM_007055.4:c.4000T>C MANE Select NP_008986.2:p.Phe1334Leu