Canonical Allele Identifier: CA450290426
Gene: POLR1C HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.43488412C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.43520674C>A , CM000668.2:g.43520674C>A GRCh38
NC_000006.11:g.43488412C>A , CM000668.1:g.43488412C>A GRCh37
NC_000006.10:g.43596390C>A NCBI36
NG_028283.1:g.8636C>A
NG_028283.3:g.15973C>A
NG_051658.1:g.60402G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000607635.2:c.705C>A ENSP00000496683.1:p.Leu235=
ENST00000642195.1:c.705C>A MANE Select ENSP00000496044.1:p.Leu235=
ENST00000643341.1:c.705C>A ENSP00000496018.1:p.Leu235=
ENST00000643799.1:c.655+247C>A ENSP00000494529.1:n.655+247C>A
ENST00000645141.1:c.*316C>A ENSP00000496755.1:n.*316C>A
ENST00000646188.1:c.540C>A ENSP00000496001.1:p.Leu180=
ENST00000646433.1:c.705C>A ENSP00000494368.1:p.Leu235=
ENST00000646700.1:c.705C>A ENSP00000495521.1:p.Leu235=
ENST00000304004.7:c.705C>A ENSP00000307212.3:p.Leu235=
ENST00000372344.6:c.655+247C>A ENSP00000361419.2:n.655+247C>A
ENST00000372389.7:c.705C>A ENSP00000361465.3:p.Leu235=
ENST00000455605.2:n.1195C>A
ENST00000481352.6:n.1077C>A
ENST00000488601.6:n.944C>A
NM_203290.2:c.705C>A NP_976035.1:p.Leu235=
XM_005249491.1:c.705C>A XP_005249548.1:p.Leu235=
XM_011515000.1:c.705C>A XP_011513302.1:p.Leu235=
NM_001318876.1:c.705C>A NP_001305805.1:p.Leu235=
NM_001363658.1:c.705C>A NP_001350587.1:p.Leu235=
NM_203290.3:c.705C>A NP_976035.1:p.Leu235=
NM_203290.4:c.705C>A MANE Select NP_976035.1:p.Leu235=
NM_001363658.2:c.705C>A NP_001350587.1:p.Leu235=
NM_001318876.2:c.705C>A NP_001305805.1:p.Leu235=