Canonical Allele Identifier: CA364284329
Gene: POLR1C HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.43520636G>T , CM000668.2:g.43520636G>T GRCh38
NC_000006.11:g.43488374G>T , CM000668.1:g.43488374G>T GRCh37
NC_000006.10:g.43596352G>T NCBI36
NG_028283.1:g.8598G>T
NG_028283.3:g.15935G>T
NG_051658.1:g.60440C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000607635.2:c.667G>T ENSP00000496683.1:p.Ala223Ser
ENST00000642195.1:c.667G>T MANE Select ENSP00000496044.1:p.Ala223Ser
ENST00000643341.1:c.667G>T ENSP00000496018.1:p.Ala223Ser
ENST00000643799.1:c.655+209G>T ENSP00000494529.1:n.655+209G>T
ENST00000645141.1:c.*278G>T ENSP00000496755.1:n.*278G>T
ENST00000646188.1:c.502G>T ENSP00000496001.1:p.Ala168Ser
ENST00000646433.1:c.667G>T ENSP00000494368.1:p.Ala223Ser
ENST00000646700.1:c.667G>T ENSP00000495521.1:p.Ala223Ser
ENST00000304004.7:c.667G>T ENSP00000307212.3:p.Ala223Ser
ENST00000372344.6:c.655+209G>T ENSP00000361419.2:n.655+209G>T
ENST00000372389.7:c.667G>T ENSP00000361465.3:p.Ala223Ser
ENST00000455605.2:n.1157G>T
ENST00000481352.6:n.1039G>T
ENST00000488601.6:n.906G>T
NM_203290.2:c.667G>T NP_976035.1:p.Ala223Ser
XM_005249491.1:c.667G>T XP_005249548.1:p.Ala223Ser
XM_011515000.1:c.667G>T XP_011513302.1:p.Ala223Ser
NM_001318876.1:c.667G>T NP_001305805.1:p.Ala223Ser
NM_001363658.1:c.667G>T NP_001350587.1:p.Ala223Ser
NM_203290.3:c.667G>T NP_976035.1:p.Ala223Ser
NM_203290.4:c.667G>T MANE Select NP_976035.1:p.Ala223Ser
NM_001363658.2:c.667G>T NP_001350587.1:p.Ala223Ser
NM_001318876.2:c.667G>T NP_001305805.1:p.Ala223Ser