Canonical Allele Identifier: CA1624610413

Gene: POLH POLR1C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.43587331G= , CM000668.2:g.43587331G=	GRCh38
NC_000006.11:g.43555068G= , CM000668.1:g.43555068G=	GRCh37
NC_000006.10:g.43663046G=	NCBI36
NG_009252.1:g.16191G= , LRG_470:g.16191G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372236.9:c.332G= (POLH) MANE Select	ENSP00000361310.4:p.Arg111=
ENST00000372226.1:c.332G= (POLH)	ENSP00000361300.1:p.Arg111=
ENST00000372236.8:c.332G= (POLH)	ENSP00000361310.4:p.Arg111=
ENST00000443535.1:c.146G= (POLH)	ENSP00000405320.1:p.Arg49=
NM_001291969.1:c.118+4190G= (POLH)	NP_001278898.1:n.118+4190G=
NM_001291970.1:c.332G= (POLH)	NP_001278899.1:p.Arg111=
NM_006502.2:c.332G= , LRG_470t1:c.332G= (POLH)	NP_006493.1:p.Arg111=
XM_005249186.2:c.146G= (POLH)	XP_005249243.1:p.Arg49=
XM_011514698.1:c.118+4190G= (POLH)	XP_011513000.1:n.118+4190G=
XM_005249186.4:c.146G= (POLH)	XP_005249243.1:p.Arg49=
XM_011514698.3:c.118+4190G= (POLH)	XP_011513000.1:n.118+4190G=
XM_024446466.1:c.80G= (POLH)	XP_024302234.1:p.Arg27=
XM_024446467.1:c.-288G= (POLH)	XP_024302235.1:n.-288G=
NM_001291969.2:c.118+4190G= (POLH)	NP_001278898.1:n.118+4190G=
NM_001291970.2:c.332G= (POLH)	NP_001278899.1:p.Arg111=
NM_006502.3:c.332G= (POLH) MANE Select	NP_006493.1:p.Arg111=
NM_001318876.2:c.945+58060G= (POLR1C)	NP_001305805.1:n.945+58060G=