Canonical Allele Identifier: CA930254281
Gene: POLR3A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.77975910_77975914del , CM000672.2:g.77975910_77975914del GRCh38
NC_000010.10:g.79735668_79735672del , CM000672.1:g.79735668_79735672del GRCh37
NC_000010.9:g.79405674_79405678del NCBI36
NG_029648.1:g.58628_58632del

Transcript Alleles

HGVS Amino-acid change
ENST00000698724.1:n.1941+4228_1941+4232del
ENST00000698725.1:n.3408_3412del
ENST00000698726.1:n.4968_4972del
ENST00000698727.1:n.4701_4705del
ENST00000698728.1:n.5317_5321del
ENST00000698729.1:n.6765_6769del
ENST00000698730.1:n.6863_6867del
ENST00000698731.1:c.*1565_*1569del ENSP00000513898.1:n.*1565_*1569del
ENST00000698732.1:c.*4427_*4431del ENSP00000513899.1:n.*4427_*4431del
ENST00000698733.1:c.*4925_*4929del ENSP00000513900.1:n.*4925_*4929del
ENST00000698734.1:c.*3911_*3915del ENSP00000513901.1:n.*3911_*3915del
ENST00000698735.1:n.6089_6093del
ENST00000698736.1:n.6502_6506del
ENST00000372371.8:c.*1565_*1569del MANE Select ENSP00000361446.3:n.*1565_*1569del
ENST00000372371.7:c.*1565_*1569del ENSP00000361446.3:n.*1565_*1569del
ENST00000616246.4:c.472+4228_472+4232del ENSP00000483738.1:n.472+4228_472+4232del
NM_007055.3:c.*1565_*1569del NP_008986.2:n.*1565_*1569del
NM_007055.4:c.*1565_*1569del MANE Select NP_008986.2:n.*1565_*1569del