Canonical Allele Identifier: CA3825451
Gene: POLR1C HGNC NCBI

Linked Data

dbSNP Id: rs755323652

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.43520177_43520189del , CM000668.2:g.43520177_43520189del GRCh38
NC_000006.11:g.43487915_43487927del , CM000668.1:g.43487915_43487927del GRCh37
NC_000006.10:g.43595893_43595905del NCBI36
NG_028283.1:g.8139_8151del
NG_028283.3:g.15476_15488del

Transcript Alleles

HGVS Amino-acid Change
ENST00000607635.2:c.494_502+4del
ENST00000642195.1:c.494_502+4del
ENST00000643341.1:c.494_502+4del
ENST00000643799.1:c.494_502+4del
ENST00000645141.1:c.*105_*113+4del
ENST00000646188.1:c.329_337+4del
ENST00000646433.1:c.494_502+4del
ENST00000646700.1:c.494_502+4del
ENST00000304004.7:c.494_502+4del
ENST00000372344.6:c.494_502+4del
ENST00000372389.7:c.494_502+4del
ENST00000423780.1:c.381-98_381-86del
ENST00000428025.6:c.329_337+4del
ENST00000455605.2:n.698_710del
ENST00000481352.6:n.777_789del
ENST00000488601.6:n.733_741+4del
NM_203290.2:c.494_502+4del
XM_005249491.1:c.494_502+4del
XM_011515000.1:c.494_502+4del
NM_001318876.1:c.494_502+4del
NM_001363658.1:c.494_502+4del
NM_203290.3:c.494_502+4del
NM_203290.4:c.494_502+4del
NM_001363658.2:c.494_502+4del
NM_001318876.2:c.494_502+4del