Canonical Allele Identifier: CA2194555587

Gene: POLG

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.89323501C= , CM000677.2:g.89323501C=	GRCh38
NC_000015.9:g.89866732C= , CM000677.1:g.89866732C=	GRCh37
NC_000015.8:g.87667736C=	NCBI36
NG_008218.1:g.16295G=
NG_008218.2:g.16295G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000636937.2:c.2168G=	ENSP00000516154.1:p.Gly723=
ENST00000268124.11:c.2168G= MANE Select	ENSP00000268124.5:p.Gly723=
ENST00000530292.3:c.1769G=	ENSP00000432885.2:p.Gly590=
ENST00000635986.2:c.2168G=	ENSP00000490653.2:p.Gly723=
ENST00000636774.1:c.*735G=	ENSP00000489799.1:n.*735G=
ENST00000637238.1:c.865G=	ENSP00000490756.1:n.865G=
ENST00000637264.1:c.1240G=
ENST00000666746.1:c.1745G=
ENST00000670281.1:c.488G=	ENSP00000499709.1:p.Gly163=
ENST00000672071.1:n.2366G=
ENST00000672923.2:n.2271G=
ENST00000268124.9:c.2168G=	ENSP00000268124.5:p.Gly723=
ENST00000442287.6:c.2168G=	ENSP00000399851.2:p.Gly723=
ENST00000526314.2:c.539+314G=
ENST00000526398.1:c.317G=
ENST00000532584.5:n.370G=
ENST00000631044.2:c.*1592G=	ENSP00000486730.1:n.*1592G=
NM_001126131.1:c.2168G=	NP_001119603.1:p.Gly723=
NM_002693.2:c.2168G=	NP_002684.1:p.Gly723=
NM_001126131.2:c.2168G=	NP_001119603.1:p.Gly723=
NM_002693.3:c.2168G= MANE Select	NP_002684.1:p.Gly723=