Canonical Allele Identifier: CA2678877229
Gene: POLR1C HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.43519690del , CM000668.2:g.43519690del GRCh38
NC_000006.11:g.43487428del , CM000668.1:g.43487428del GRCh37
NC_000006.10:g.43595406del NCBI36
NG_028283.1:g.7652del
NG_028283.3:g.14989del

Transcript Alleles

HGVS Amino-acid Change
ENST00000607635.2:c.250-16del ENSP00000496683.1:n.250-16del
ENST00000642195.1:c.250-16del MANE Select ENSP00000496044.1:n.250-16del
ENST00000643341.1:c.250-16del ENSP00000496018.1:n.250-16del
ENST00000643799.1:c.250-16del ENSP00000494529.1:n.250-16del
ENST00000645141.1:c.250-16del ENSP00000496755.1:n.250-16del
ENST00000646188.1:c.85-16del ENSP00000496001.1:n.85-16del
ENST00000646433.1:c.250-16del ENSP00000494368.1:n.250-16del
ENST00000646700.1:c.250-16del ENSP00000495521.1:n.250-16del
ENST00000304004.7:c.250-16del ENSP00000307212.3:n.250-16del
ENST00000372344.6:c.250-16del ENSP00000361419.2:n.250-16del
ENST00000372389.7:c.250-16del ENSP00000361465.3:n.250-16del
ENST00000423780.1:c.248-16del
ENST00000428025.6:c.85-16del ENSP00000395401.2:n.85-16del
ENST00000455605.2:n.227-16del
ENST00000481352.6:n.306-16del
ENST00000488601.6:n.262-16del
ENST00000512472.5:n.526del
NM_203290.2:c.250-16del NP_976035.1:n.250-16del
XM_005249491.1:c.250-16del XP_005249548.1:n.250-16del
XM_011515000.1:c.250-16del XP_011513302.1:n.250-16del
NM_001318876.1:c.250-16del NP_001305805.1:n.250-16del
NM_001363658.1:c.250-16del NP_001350587.1:n.250-16del
NM_203290.3:c.250-16del NP_976035.1:n.250-16del
NM_203290.4:c.250-16del MANE Select NP_976035.1:n.250-16del
NM_001363658.2:c.250-16del NP_001350587.1:n.250-16del
NM_001318876.2:c.250-16del NP_001305805.1:n.250-16del