Canonical Allele Identifier: CA2678869137
Gene: POLR1C HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.43519897_43519898del , CM000668.2:g.43519897_43519898del GRCh38
NC_000006.11:g.43487635_43487636del , CM000668.1:g.43487635_43487636del GRCh37
NC_000006.10:g.43595613_43595614del NCBI36
NG_028283.1:g.7859_7860del
NG_028283.3:g.15196_15197del

Transcript Alleles

HGVS Amino-acid Change
ENST00000607635.2:c.382+59_382+60del ENSP00000496683.1:n.382+59_382+60del
ENST00000642195.1:c.382+59_382+60del MANE Select ENSP00000496044.1:n.382+59_382+60del
ENST00000643341.1:c.382+59_382+60del ENSP00000496018.1:n.382+59_382+60del
ENST00000643799.1:c.382+59_382+60del ENSP00000494529.1:n.382+59_382+60del
ENST00000645141.1:c.441_442del ENSP00000496755.1:p.Cys147Ter
ENST00000646188.1:c.217+59_217+60del ENSP00000496001.1:n.217+59_217+60del
ENST00000646433.1:c.382+59_382+60del ENSP00000494368.1:n.382+59_382+60del
ENST00000646700.1:c.382+59_382+60del ENSP00000495521.1:n.382+59_382+60del
ENST00000304004.7:c.382+59_382+60del ENSP00000307212.3:n.382+59_382+60del
ENST00000372344.6:c.382+59_382+60del ENSP00000361419.2:n.382+59_382+60del
ENST00000372389.7:c.382+59_382+60del ENSP00000361465.3:n.382+59_382+60del
ENST00000423780.1:c.380+59_380+60del
ENST00000428025.6:c.217+59_217+60del ENSP00000395401.2:n.217+59_217+60del
ENST00000455605.2:n.418_419del
ENST00000481352.6:n.497_498del
ENST00000488601.6:n.453_454del
NM_203290.2:c.382+59_382+60del NP_976035.1:n.382+59_382+60del
XM_005249491.1:c.382+59_382+60del XP_005249548.1:n.382+59_382+60del
XM_011515000.1:c.382+59_382+60del XP_011513302.1:n.382+59_382+60del
NM_001318876.1:c.382+59_382+60del NP_001305805.1:n.382+59_382+60del
NM_001363658.1:c.382+59_382+60del NP_001350587.1:n.382+59_382+60del
NM_203290.3:c.382+59_382+60del NP_976035.1:n.382+59_382+60del
NM_203290.4:c.382+59_382+60del MANE Select NP_976035.1:n.382+59_382+60del
NM_001363658.2:c.382+59_382+60del NP_001350587.1:n.382+59_382+60del
NM_001318876.2:c.382+59_382+60del NP_001305805.1:n.382+59_382+60del