Canonical Allele Identifier: CA450290600
Gene: POLR1C HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.43488454A>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.43520716A>C , CM000668.2:g.43520716A>C GRCh38
NC_000006.11:g.43488454A>C , CM000668.1:g.43488454A>C GRCh37
NC_000006.10:g.43596432A>C NCBI36
NG_028283.1:g.8678A>C
NG_028283.3:g.16015A>C
NG_051658.1:g.60360T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000607635.2:c.747A>C ENSP00000496683.1:p.Ala249=
ENST00000642195.1:c.747A>C MANE Select ENSP00000496044.1:p.Ala249=
ENST00000643341.1:c.747A>C ENSP00000496018.1:p.Ala249=
ENST00000643799.1:c.656-216A>C ENSP00000494529.1:n.656-216A>C
ENST00000645141.1:c.*358A>C ENSP00000496755.1:n.*358A>C
ENST00000646188.1:c.582A>C ENSP00000496001.1:p.Ala194=
ENST00000646433.1:c.747A>C ENSP00000494368.1:p.Ala249=
ENST00000646700.1:c.747A>C ENSP00000495521.1:p.Ala249=
ENST00000304004.7:c.747A>C ENSP00000307212.3:p.Ala249=
ENST00000372344.6:c.656-216A>C ENSP00000361419.2:n.656-216A>C
ENST00000372389.7:c.747A>C ENSP00000361465.3:p.Ala249=
ENST00000455605.2:n.1237A>C
ENST00000481352.6:n.1119A>C
NM_203290.2:c.747A>C NP_976035.1:p.Ala249=
XM_005249491.1:c.747A>C XP_005249548.1:p.Ala249=
XM_011515000.1:c.747A>C XP_011513302.1:p.Ala249=
NM_001318876.1:c.747A>C NP_001305805.1:p.Ala249=
NM_001363658.1:c.747A>C NP_001350587.1:p.Ala249=
NM_203290.3:c.747A>C NP_976035.1:p.Ala249=
NM_203290.4:c.747A>C MANE Select NP_976035.1:p.Ala249=
NM_001363658.2:c.747A>C NP_001350587.1:p.Ala249=
NM_001318876.2:c.747A>C NP_001305805.1:p.Ala249=