Canonical Allele Identifier: CA364283607
Gene: POLR1C HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.43520171A>G , CM000668.2:g.43520171A>G GRCh38
NC_000006.11:g.43487909A>G , CM000668.1:g.43487909A>G GRCh37
NC_000006.10:g.43595887A>G NCBI36
NG_028283.1:g.8133A>G
NG_028283.3:g.15470A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000607635.2:c.488A>G ENSP00000496683.1:p.Tyr163Cys
ENST00000642195.1:c.488A>G MANE Select ENSP00000496044.1:p.Tyr163Cys
ENST00000643341.1:c.488A>G ENSP00000496018.1:p.Tyr163Cys
ENST00000643799.1:c.488A>G ENSP00000494529.1:p.Tyr163Cys
ENST00000645141.1:c.*99A>G ENSP00000496755.1:n.*99A>G
ENST00000646188.1:c.323A>G ENSP00000496001.1:p.Tyr108Cys
ENST00000646433.1:c.488A>G ENSP00000494368.1:p.Tyr163Cys
ENST00000646700.1:c.488A>G ENSP00000495521.1:p.Tyr163Cys
ENST00000304004.7:c.488A>G ENSP00000307212.3:p.Tyr163Cys
ENST00000372344.6:c.488A>G ENSP00000361419.2:p.Tyr163Cys
ENST00000372389.7:c.488A>G ENSP00000361465.3:p.Tyr163Cys
ENST00000423780.1:c.381-104A>G
ENST00000428025.6:c.323A>G ENSP00000395401.2:p.Tyr108Cys
ENST00000455605.2:n.692A>G
ENST00000481352.6:n.771A>G
ENST00000488601.6:n.727A>G
NM_203290.2:c.488A>G NP_976035.1:p.Tyr163Cys
XM_005249491.1:c.488A>G XP_005249548.1:p.Tyr163Cys
XM_011515000.1:c.488A>G XP_011513302.1:p.Tyr163Cys
NM_001318876.1:c.488A>G NP_001305805.1:p.Tyr163Cys
NM_001363658.1:c.488A>G NP_001350587.1:p.Tyr163Cys
NM_203290.3:c.488A>G NP_976035.1:p.Tyr163Cys
NM_203290.4:c.488A>G MANE Select NP_976035.1:p.Tyr163Cys
NM_001363658.2:c.488A>G NP_001350587.1:p.Tyr163Cys
NM_001318876.2:c.488A>G NP_001305805.1:p.Tyr163Cys