Canonical Allele Identifier: CA1624558395

Gene: POLR1C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.43519782G= , CM000668.2:g.43519782G=	GRCh38
NC_000006.11:g.43487520G= , CM000668.1:g.43487520G=	GRCh37
NC_000006.10:g.43595498G=	NCBI36
NG_028283.1:g.7744G=
NG_028283.3:g.15081G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000607635.2:c.326G=	ENSP00000496683.1:p.Arg109=
ENST00000642195.1:c.326G= MANE Select	ENSP00000496044.1:p.Arg109=
ENST00000643341.1:c.326G=	ENSP00000496018.1:p.Arg109=
ENST00000643799.1:c.326G=	ENSP00000494529.1:p.Arg109=
ENST00000645141.1:c.326G=	ENSP00000496755.1:p.Arg109=
ENST00000646188.1:c.161G=	ENSP00000496001.1:p.Arg54=
ENST00000646433.1:c.326G=	ENSP00000494368.1:p.Arg109=
ENST00000646700.1:c.326G=	ENSP00000495521.1:p.Arg109=
ENST00000304004.7:c.326G=	ENSP00000307212.3:p.Arg109=
ENST00000372344.6:c.326G=	ENSP00000361419.2:p.Arg109=
ENST00000372389.7:c.326G=	ENSP00000361465.3:p.Arg109=
ENST00000423780.1:c.324G=
ENST00000428025.6:c.161G=	ENSP00000395401.2:p.Arg54=
ENST00000455605.2:n.303G=
ENST00000481352.6:n.382G=
ENST00000488601.6:n.338G=
NM_203290.2:c.326G=	NP_976035.1:p.Arg109=
XM_005249491.1:c.326G=	XP_005249548.1:p.Arg109=
XM_011515000.1:c.326G=	XP_011513302.1:p.Arg109=
NM_001318876.1:c.326G=	NP_001305805.1:p.Arg109=
NM_001363658.1:c.326G=	NP_001350587.1:p.Arg109=
NM_203290.3:c.326G=	NP_976035.1:p.Arg109=
NM_203290.4:c.326G= MANE Select	NP_976035.1:p.Arg109=
NM_001363658.2:c.326G=	NP_001350587.1:p.Arg109=
NM_001318876.2:c.326G=	NP_001305805.1:p.Arg109=