Canonical Allele Identifier: CA2194550553

Gene: POLG

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.89321779C= , CM000677.2:g.89321779C=	GRCh38
NC_000015.9:g.89865010C= , CM000677.1:g.89865010C=	GRCh37
NC_000015.8:g.87666014C=	NCBI36
NG_008218.1:g.18017G=
NG_008218.2:g.18017G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000636937.2:c.2555G=	ENSP00000516154.1:p.Arg852=
ENST00000268124.11:c.2555G= MANE Select	ENSP00000268124.5:p.Arg852=
ENST00000530292.3:c.2156G=	ENSP00000432885.2:p.Arg719=
ENST00000635986.2:c.2555G=	ENSP00000490653.2:p.Arg852=
ENST00000636774.1:c.*1122G=	ENSP00000489799.1:n.*1122G=
ENST00000637238.1:c.1252G=	ENSP00000490756.1:n.1252G=
ENST00000637264.1:c.1627G=
ENST00000666746.1:c.2132G=
ENST00000670281.1:c.800+183G=	ENSP00000499709.1:n.800+183G=
ENST00000672071.1:n.2753G=
ENST00000672923.2:n.2497G=
ENST00000268124.9:c.2555G=	ENSP00000268124.5:p.Arg852=
ENST00000442287.6:c.2555G=	ENSP00000399851.2:p.Arg852=
ENST00000528881.2:c.196-519G=
ENST00000530715.5:c.186-910G=	ENSP00000431395.1:n.186-910G=
ENST00000532584.5:n.704G=
ENST00000631044.2:c.*1979G=	ENSP00000486730.1:n.*1979G=
NM_001126131.1:c.2555G=	NP_001119603.1:p.Arg852=
NM_002693.2:c.2555G=	NP_002684.1:p.Arg852=
NM_001126131.2:c.2555G=	NP_001119603.1:p.Arg852=
NM_002693.3:c.2555G= MANE Select	NP_002684.1:p.Arg852=