Canonical Allele Identifier: CA2194542003

Gene: POLG

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.89318681C= , CM000677.2:g.89318681C=	GRCh38
NC_000015.9:g.89861912C= , CM000677.1:g.89861912C=	GRCh37
NC_000015.8:g.87662916C=	NCBI36
NG_008218.1:g.21115G=
NG_011736.1:g.79719C= , LRG_500:g.79719C=
NG_008218.2:g.21115G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000636937.2:c.3342G=	ENSP00000516154.1:p.Val1114=
ENST00000268124.11:c.3342G= MANE Select	ENSP00000268124.5:p.Val1114=
ENST00000530292.3:c.2943G=	ENSP00000432885.2:p.Val981=
ENST00000635986.2:c.*412G=	ENSP00000490653.2:n.*412G=
ENST00000636774.1:c.*1909G=	ENSP00000489799.1:n.*1909G=
ENST00000637238.1:c.2151G=	ENSP00000490756.1:n.2151G=
ENST00000637264.1:c.2414G=
ENST00000666746.1:c.2919G=
ENST00000672071.1:n.3540G=
ENST00000672695.1:n.519G=
ENST00000672923.2:n.3342G=
ENST00000268124.9:c.3342G=	ENSP00000268124.5:p.Val1114=
ENST00000442287.6:c.3342G=	ENSP00000399851.2:p.Val1114=
ENST00000530292.2:c.426G=	ENSP00000432885.1:p.Val142=
ENST00000631044.2:c.*2766G=	ENSP00000486730.1:n.*2766G=
NM_001126131.1:c.3342G=	NP_001119603.1:p.Val1114=
NM_002693.2:c.3342G=	NP_002684.1:p.Val1114=
NM_001126131.2:c.3342G=	NP_001119603.1:p.Val1114=
NM_002693.3:c.3342G= MANE Select	NP_002684.1:p.Val1114=