Canonical Allele Identifier: CA1624558910
Gene: POLR1C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.43520173G= , CM000668.2:g.43520173G= GRCh38
NC_000006.11:g.43487911G= , CM000668.1:g.43487911G= GRCh37
NC_000006.10:g.43595889G= NCBI36
NG_028283.1:g.8135G=
NG_028283.3:g.15472G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000607635.2:c.490G= ENSP00000496683.1:p.Val164=
ENST00000642195.1:c.490G= MANE Select ENSP00000496044.1:p.Val164=
ENST00000643341.1:c.490G= ENSP00000496018.1:p.Val164=
ENST00000643799.1:c.490G= ENSP00000494529.1:p.Val164=
ENST00000645141.1:c.*101G= ENSP00000496755.1:n.*101G=
ENST00000646188.1:c.325G= ENSP00000496001.1:p.Val109=
ENST00000646433.1:c.490G= ENSP00000494368.1:p.Val164=
ENST00000646700.1:c.490G= ENSP00000495521.1:p.Val164=
ENST00000304004.7:c.490G= ENSP00000307212.3:p.Val164=
ENST00000372344.6:c.490G= ENSP00000361419.2:p.Val164=
ENST00000372389.7:c.490G= ENSP00000361465.3:p.Val164=
ENST00000423780.1:c.381-102G=
ENST00000428025.6:c.325G= ENSP00000395401.2:p.Val109=
ENST00000455605.2:n.694G=
ENST00000481352.6:n.773G=
ENST00000488601.6:n.729G=
NM_203290.2:c.490G= NP_976035.1:p.Val164=
XM_005249491.1:c.490G= XP_005249548.1:p.Val164=
XM_011515000.1:c.490G= XP_011513302.1:p.Val164=
NM_001318876.1:c.490G= NP_001305805.1:p.Val164=
NM_001363658.1:c.490G= NP_001350587.1:p.Val164=
NM_203290.3:c.490G= NP_976035.1:p.Val164=
NM_203290.4:c.490G= MANE Select NP_976035.1:p.Val164=
NM_001363658.2:c.490G= NP_001350587.1:p.Val164=
NM_001318876.2:c.490G= NP_001305805.1:p.Val164=