Canonical Allele Identifier: CA2805170402
Gene: POLG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.89325728_89325729insACAC , CM000677.2:g.89325728_89325729insACAC GRCh38
NC_000015.9:g.89868959_89868960insACAC , CM000677.1:g.89868959_89868960insACAC GRCh37
NC_000015.8:g.87669963_87669964insACAC NCBI36
NG_008218.1:g.14067_14068insGTGT
NG_008218.2:g.14067_14068insGTGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000636937.2:c.1713-43_1713-42insGTGT ENSP00000516154.1:n.1713-43_1713-42insGTGT
ENST00000268124.11:c.1713-43_1713-42insGTGT MANE Select ENSP00000268124.5:n.1713-43_1713-42insGTGT
ENST00000530292.3:c.1314-43_1314-42insGTGT ENSP00000432885.2:n.1314-43_1314-42insGTGT
ENST00000635986.2:c.1713-43_1713-42insGTGT ENSP00000490653.2:n.1713-43_1713-42insGTGT
ENST00000636774.1:c.*280-43_*280-42insGTGT ENSP00000489799.1:n.*280-43_*280-42insGTGT
ENST00000637238.1:c.450-43_450-42insGTGT ENSP00000490756.1:n.450-43_450-42insGTGT
ENST00000637264.1:c.785-43_785-42insGTGT
ENST00000666746.1:c.1290-43_1290-42insGTGT
ENST00000670281.1:c.33-43_33-42insGTGT ENSP00000499709.1:n.33-43_33-42insGTGT
ENST00000672071.1:n.1911-43_1911-42insGTGT
ENST00000672923.2:n.1816-43_1816-42insGTGT
ENST00000268124.9:c.1713-43_1713-42insGTGT ENSP00000268124.5:n.1713-43_1713-42insGTGT
ENST00000442287.6:c.1713-43_1713-42insGTGT ENSP00000399851.2:n.1713-43_1713-42insGTGT
ENST00000526314.2:c.95-43_95-42insGTGT
ENST00000631044.2:c.*1096-43_*1096-42insGTGT ENSP00000486730.1:n.*1096-43_*1096-42insGTGT
NM_001126131.1:c.1713-43_1713-42insGTGT NP_001119603.1:n.1713-43_1713-42insGTGT
NM_002693.2:c.1713-43_1713-42insGTGT NP_002684.1:n.1713-43_1713-42insGTGT
NM_001126131.2:c.1713-43_1713-42insGTGT NP_001119603.1:n.1713-43_1713-42insGTGT
NM_002693.3:c.1713-43_1713-42insGTGT MANE Select NP_002684.1:n.1713-43_1713-42insGTGT