Canonical Allele Identifier: CA259909
Gene: POLR1C HGNC NCBI
MyVariant.info:
Revel Score:
gnomAD v4:

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.43520962G>A , CM000668.2:g.43520962G>A GRCh38
NC_000006.11:g.43488700G>A , CM000668.1:g.43488700G>A GRCh37
NC_000006.10:g.43596678G>A NCBI36
NG_028283.1:g.8924G>A
NG_028283.3:g.16261G>A
NG_051658.1:g.60114C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000607635.2:c.836G>A ENSP00000496683.1:p.Arg279Gln
ENST00000642195.1:c.836G>A MANE Select ENSP00000496044.1:p.Arg279Gln
ENST00000643341.1:c.836G>A ENSP00000496018.1:p.Arg279Gln
ENST00000643799.1:c.686G>A ENSP00000494529.1:p.Arg229Gln
ENST00000645141.1:c.*447G>A ENSP00000496755.1:n.*447G>A
ENST00000646188.1:c.671G>A ENSP00000496001.1:p.Arg224Gln
ENST00000646433.1:c.836G>A ENSP00000494368.1:p.Arg279Gln
ENST00000646700.1:c.836G>A ENSP00000495521.1:p.Arg279Gln
ENST00000304004.7:c.836G>A ENSP00000307212.3:p.Arg279Gln
ENST00000372344.6:c.686G>A ENSP00000361419.2:p.Arg229Gln
ENST00000372389.7:c.836G>A ENSP00000361465.3:p.Arg279Gln
ENST00000455605.2:n.1483G>A
ENST00000481352.6:n.1208G>A
NM_203290.2:c.836G>A NP_976035.1:p.Arg279Gln
XM_005249491.1:c.836G>A XP_005249548.1:p.Arg279Gln
XM_011515000.1:c.836G>A XP_011513302.1:p.Arg279Gln
NM_001318876.1:c.836G>A NP_001305805.1:p.Arg279Gln
NM_001363658.1:c.836G>A NP_001350587.1:p.Arg279Gln
NM_203290.3:c.836G>A NP_976035.1:p.Arg279Gln
NM_203290.4:c.836G>A MANE Select NP_976035.1:p.Arg279Gln
NM_001363658.2:c.836G>A NP_001350587.1:p.Arg279Gln
NM_001318876.2:c.836G>A NP_001305805.1:p.Arg279Gln