Canonical Allele Identifier: CA364283666
Gene: POLR1C HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.43520281C>T , CM000668.2:g.43520281C>T GRCh38
NC_000006.11:g.43488019C>T , CM000668.1:g.43488019C>T GRCh37
NC_000006.10:g.43595997C>T NCBI36
NG_028283.1:g.8243C>T
NG_028283.3:g.15580C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000607635.2:c.509C>T ENSP00000496683.1:p.Thr170Ile
ENST00000642195.1:c.509C>T MANE Select ENSP00000496044.1:p.Thr170Ile
ENST00000643341.1:c.509C>T ENSP00000496018.1:p.Thr170Ile
ENST00000643799.1:c.509C>T ENSP00000494529.1:p.Thr170Ile
ENST00000645141.1:c.*120C>T ENSP00000496755.1:n.*120C>T
ENST00000646188.1:c.344C>T ENSP00000496001.1:p.Thr115Ile
ENST00000646433.1:c.509C>T ENSP00000494368.1:p.Thr170Ile
ENST00000646700.1:c.509C>T ENSP00000495521.1:p.Thr170Ile
ENST00000304004.7:c.509C>T ENSP00000307212.3:p.Thr170Ile
ENST00000372344.6:c.509C>T ENSP00000361419.2:p.Thr170Ile
ENST00000372389.7:c.509C>T ENSP00000361465.3:p.Thr170Ile
ENST00000423780.1:c.387C>T
ENST00000428025.6:c.344C>T ENSP00000395401.2:p.Thr115Ile
ENST00000455605.2:n.802C>T
ENST00000481352.6:n.881C>T
ENST00000488601.6:n.748C>T
NM_203290.2:c.509C>T NP_976035.1:p.Thr170Ile
XM_005249491.1:c.509C>T XP_005249548.1:p.Thr170Ile
XM_011515000.1:c.509C>T XP_011513302.1:p.Thr170Ile
NM_001318876.1:c.509C>T NP_001305805.1:p.Thr170Ile
NM_001363658.1:c.509C>T NP_001350587.1:p.Thr170Ile
NM_203290.3:c.509C>T NP_976035.1:p.Thr170Ile
NM_203290.4:c.509C>T MANE Select NP_976035.1:p.Thr170Ile
NM_001363658.2:c.509C>T NP_001350587.1:p.Thr170Ile
NM_001318876.2:c.509C>T NP_001305805.1:p.Thr170Ile