Canonical Allele Identifier: CA2194550101

Gene: POLG

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.89325520G= , CM000677.2:g.89325520G=	GRCh38
NC_000015.9:g.89868751G= , CM000677.1:g.89868751G=	GRCh37
NC_000015.8:g.87669755G=	NCBI36
NG_008218.1:g.14276C=
NG_008218.2:g.14276C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000636937.2:c.1879C=	ENSP00000516154.1:p.Arg627=
ENST00000268124.11:c.1879C= MANE Select	ENSP00000268124.5:p.Arg627=
ENST00000530292.3:c.1480C=	ENSP00000432885.2:p.Arg494=
ENST00000635986.2:c.1879C=	ENSP00000490653.2:p.Arg627=
ENST00000636774.1:c.*446C=	ENSP00000489799.1:n.*446C=
ENST00000637238.1:c.616C=	ENSP00000490756.1:p.Arg206=
ENST00000637264.1:c.951C=
ENST00000666746.1:c.1456C=
ENST00000670281.1:c.199C=	ENSP00000499709.1:p.Arg67=
ENST00000672071.1:n.2077C=
ENST00000672923.2:n.1982C=
ENST00000268124.9:c.1879C=	ENSP00000268124.5:p.Arg627=
ENST00000442287.6:c.1879C=	ENSP00000399851.2:p.Arg627=
ENST00000526314.2:c.261C=
ENST00000526398.1:c.68C=
ENST00000532584.5:n.81C=
ENST00000631044.2:c.*1262C=	ENSP00000486730.1:n.*1262C=
NM_001126131.1:c.1879C=	NP_001119603.1:p.Arg627=
NM_002693.2:c.1879C=	NP_002684.1:p.Arg627=
NM_001126131.2:c.1879C=	NP_001119603.1:p.Arg627=
NM_002693.3:c.1879C= MANE Select	NP_002684.1:p.Arg627=