Canonical Allele Identifier: CA2519564319

Gene: POLR1C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.43519848_43519849insCTCATCCT , CM000668.2:g.43519848_43519849insCTCATCCT	GRCh38
NC_000006.11:g.43487586_43487587insCTCATCCT , CM000668.1:g.43487586_43487587insCTCATCCT	GRCh37
NC_000006.10:g.43595564_43595565insCTCATCCT	NCBI36
NG_028283.1:g.7810_7811insCTCATCCT
NG_028283.3:g.15147_15148insCTCATCCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000607635.2:c.382+10_382+11insCTCATCCT	ENSP00000496683.1:n.382+10_382+11insCTCATCCT
ENST00000642195.1:c.382+10_382+11insCTCATCCT MANE Select	ENSP00000496044.1:n.382+10_382+11insCTCATCCT
ENST00000643341.1:c.382+10_382+11insCTCATCCT	ENSP00000496018.1:n.382+10_382+11insCTCATCCT
ENST00000643799.1:c.382+10_382+11insCTCATCCT	ENSP00000494529.1:n.382+10_382+11insCTCATCCT
ENST00000645141.1:c.392_393insCTCATCCT	ENSP00000496755.1:p.Met131IlefsTer4
ENST00000646188.1:c.217+10_217+11insCTCATCCT	ENSP00000496001.1:n.217+10_217+11insCTCATCCT
ENST00000646433.1:c.382+10_382+11insCTCATCCT	ENSP00000494368.1:n.382+10_382+11insCTCATCCT
ENST00000646700.1:c.382+10_382+11insCTCATCCT	ENSP00000495521.1:n.382+10_382+11insCTCATCCT
ENST00000304004.7:c.382+10_382+11insCTCATCCT	ENSP00000307212.3:n.382+10_382+11insCTCATCCT
ENST00000372344.6:c.382+10_382+11insCTCATCCT	ENSP00000361419.2:n.382+10_382+11insCTCATCCT
ENST00000372389.7:c.382+10_382+11insCTCATCCT	ENSP00000361465.3:n.382+10_382+11insCTCATCCT
ENST00000423780.1:c.380+10_380+11insCTCATCCT
ENST00000428025.6:c.217+10_217+11insCTCATCCT	ENSP00000395401.2:n.217+10_217+11insCTCATCCT
ENST00000455605.2:n.369_370insCTCATCCT
ENST00000481352.6:n.448_449insCTCATCCT
ENST00000488601.6:n.404_405insCTCATCCT
NM_203290.2:c.382+10_382+11insCTCATCCT	NP_976035.1:n.382+10_382+11insCTCATCCT
XM_005249491.1:c.382+10_382+11insCTCATCCT	XP_005249548.1:n.382+10_382+11insCTCATCCT
XM_011515000.1:c.382+10_382+11insCTCATCCT	XP_011513302.1:n.382+10_382+11insCTCATCCT
NM_001318876.1:c.382+10_382+11insCTCATCCT	NP_001305805.1:n.382+10_382+11insCTCATCCT
NM_001363658.1:c.382+10_382+11insCTCATCCT	NP_001350587.1:n.382+10_382+11insCTCATCCT
NM_203290.3:c.382+10_382+11insCTCATCCT	NP_976035.1:n.382+10_382+11insCTCATCCT
NM_203290.4:c.382+10_382+11insCTCATCCT MANE Select	NP_976035.1:n.382+10_382+11insCTCATCCT
NM_001363658.2:c.382+10_382+11insCTCATCCT	NP_001350587.1:n.382+10_382+11insCTCATCCT
NM_001318876.2:c.382+10_382+11insCTCATCCT	NP_001305805.1:n.382+10_382+11insCTCATCCT