Canonical Allele Identifier: CA2609821164
Gene: POLR3A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.77980179_77980180del , CM000672.2:g.77980179_77980180del GRCh38
NC_000010.10:g.79739937_79739938del , CM000672.1:g.79739937_79739938del GRCh37
NC_000010.9:g.79409943_79409944del NCBI36
NG_029648.1:g.54362_54363del

Transcript Alleles

HGVS Amino-acid Change
ENST00000698724.1:n.1903_1904del
ENST00000698725.1:n.1656_1657del
ENST00000698726.1:n.3216_3217del
ENST00000698727.1:n.2949_2950del
ENST00000698728.1:n.3565_3566del
ENST00000698729.1:n.5013_5014del
ENST00000698730.1:n.5111_5112del
ENST00000698731.1:c.3845_3846del ENSP00000513898.1:p.Phe1282Ter
ENST00000698732.1:c.*2675_*2676del ENSP00000513899.1:n.*2675_*2676del
ENST00000698733.1:c.*3173_*3174del ENSP00000513900.1:n.*3173_*3174del
ENST00000698734.1:c.*2159_*2160del ENSP00000513901.1:n.*2159_*2160del
ENST00000698735.1:n.4337_4338del
ENST00000698736.1:n.4750_4751del
ENST00000698737.1:n.4101_4102del
ENST00000372371.8:c.3986_3987del MANE Select ENSP00000361446.3:p.Phe1329Ter
ENST00000372371.7:c.3986_3987del ENSP00000361446.3:p.Phe1329Ter
ENST00000616246.4:c.434_435del ENSP00000483738.1:p.Phe145Ter
NM_007055.3:c.3986_3987del NP_008986.2:p.Phe1329Ter
NM_007055.4:c.3986_3987del MANE Select NP_008986.2:p.Phe1329Ter