Canonical Allele Identifier: CA1624559696

Gene: POLR1C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.43520657A= , CM000668.2:g.43520657A=	GRCh38
NC_000006.11:g.43488395A= , CM000668.1:g.43488395A=	GRCh37
NC_000006.10:g.43596373A=	NCBI36
NG_028283.1:g.8619A=
NG_028283.3:g.15956A=
NG_051658.1:g.60419T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000607635.2:c.688A=	ENSP00000496683.1:p.Thr230=
ENST00000642195.1:c.688A= MANE Select	ENSP00000496044.1:p.Thr230=
ENST00000643341.1:c.688A=	ENSP00000496018.1:p.Thr230=
ENST00000643799.1:c.655+230A=	ENSP00000494529.1:n.655+230A=
ENST00000645141.1:c.*299A=	ENSP00000496755.1:n.*299A=
ENST00000646188.1:c.523A=	ENSP00000496001.1:p.Thr175=
ENST00000646433.1:c.688A=	ENSP00000494368.1:p.Thr230=
ENST00000646700.1:c.688A=	ENSP00000495521.1:p.Thr230=
ENST00000304004.7:c.688A=	ENSP00000307212.3:p.Thr230=
ENST00000372344.6:c.655+230A=	ENSP00000361419.2:n.655+230A=
ENST00000372389.7:c.688A=	ENSP00000361465.3:p.Thr230=
ENST00000455605.2:n.1178A=
ENST00000481352.6:n.1060A=
ENST00000488601.6:n.927A=
NM_203290.2:c.688A=	NP_976035.1:p.Thr230=
XM_005249491.1:c.688A=	XP_005249548.1:p.Thr230=
XM_011515000.1:c.688A=	XP_011513302.1:p.Thr230=
NM_001318876.1:c.688A=	NP_001305805.1:p.Thr230=
NM_001363658.1:c.688A=	NP_001350587.1:p.Thr230=
NM_203290.3:c.688A=	NP_976035.1:p.Thr230=
NM_203290.4:c.688A= MANE Select	NP_976035.1:p.Thr230=
NM_001363658.2:c.688A=	NP_001350587.1:p.Thr230=
NM_001318876.2:c.688A=	NP_001305805.1:p.Thr230=