Canonical Allele Identifier: CA2609821213
Gene: POLR3A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.77980332_77980337del , CM000672.2:g.77980332_77980337del GRCh38
NC_000010.10:g.79740090_79740095del , CM000672.1:g.79740090_79740095del GRCh37
NC_000010.9:g.79410096_79410101del NCBI36
NG_029648.1:g.54205_54210del

Transcript Alleles

HGVS Amino-acid Change
ENST00000698724.1:n.1809-63_1809-58del
ENST00000698725.1:n.1499_1504del
ENST00000698726.1:n.3122-63_3122-58del
ENST00000698727.1:n.2855-63_2855-58del
ENST00000698728.1:n.3471-63_3471-58del
ENST00000698729.1:n.4919-63_4919-58del
ENST00000698730.1:n.5017-63_5017-58del
ENST00000698731.1:c.3751-63_3751-58del ENSP00000513898.1:n.3751-63_3751-58del
ENST00000698732.1:c.*2581-63_*2581-58del ENSP00000513899.1:n.*2581-63_*2581-58del
ENST00000698733.1:c.*3079-63_*3079-58del ENSP00000513900.1:n.*3079-63_*3079-58del
ENST00000698734.1:c.*2065-63_*2065-58del ENSP00000513901.1:n.*2065-63_*2065-58del
ENST00000698735.1:n.4243-63_4243-58del
ENST00000698736.1:n.4656-63_4656-58del
ENST00000698737.1:n.4007-63_4007-58del
ENST00000372371.8:c.3892-63_3892-58del MANE Select ENSP00000361446.3:n.3892-63_3892-58del
ENST00000372371.7:c.3892-63_3892-58del ENSP00000361446.3:n.3892-63_3892-58del
ENST00000616246.4:c.340-63_340-58del ENSP00000483738.1:n.340-63_340-58del
NM_007055.3:c.3892-63_3892-58del NP_008986.2:n.3892-63_3892-58del
NM_007055.4:c.3892-63_3892-58del MANE Select NP_008986.2:n.3892-63_3892-58del