Canonical Allele Identifier: CA2194539476

Gene: POLG

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.89317514C= , CM000677.2:g.89317514C=	GRCh38
NC_000015.9:g.89860745C= , CM000677.1:g.89860745C=	GRCh37
NC_000015.8:g.87661749C=	NCBI36
NG_008218.1:g.22282G=
NG_011736.1:g.78552C= , LRG_500:g.78552C=
NG_008218.2:g.22282G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000636937.2:c.3505G=	ENSP00000516154.1:p.Gly1169=
ENST00000268124.11:c.3505G= MANE Select	ENSP00000268124.5:p.Gly1169=
ENST00000530292.3:c.3205G=	ENSP00000432885.2:n.3205G=
ENST00000635986.2:c.*575G=	ENSP00000490653.2:n.*575G=
ENST00000636774.1:c.*2109G=	ENSP00000489799.1:n.*2109G=
ENST00000637042.1:n.72-43G=
ENST00000637238.1:c.2413G=	ENSP00000490756.1:n.2413G=
ENST00000637264.1:c.2555-38G=
ENST00000666746.1:c.3082G=
ENST00000672071.1:n.4707G=
ENST00000672695.1:n.1284G=
ENST00000672923.2:n.3505G=
ENST00000268124.9:c.3505G=	ENSP00000268124.5:p.Gly1169=
ENST00000442287.6:c.3505G=	ENSP00000399851.2:p.Gly1169=
ENST00000526671.1:n.315G=
ENST00000530292.2:c.688G=	ENSP00000432885.1:n.688G=
ENST00000631044.2:c.*2929G=	ENSP00000486730.1:n.*2929G=
NM_001126131.1:c.3505G=	NP_001119603.1:p.Gly1169=
NM_002693.2:c.3505G=	NP_002684.1:p.Gly1169=
NM_001126131.2:c.3505G=	NP_001119603.1:p.Gly1169=
NM_002693.3:c.3505G= MANE Select	NP_002684.1:p.Gly1169=