Canonical Allele Identifier: CA2805170405
Gene: POLG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.89325731_89325732insACA , CM000677.2:g.89325731_89325732insACA GRCh38
NC_000015.9:g.89868962_89868963insACA , CM000677.1:g.89868962_89868963insACA GRCh37
NC_000015.8:g.87669966_87669967insACA NCBI36
NG_008218.1:g.14064_14065insTGT
NG_008218.2:g.14064_14065insTGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000636937.2:c.1713-46_1713-45insTGT ENSP00000516154.1:n.1713-46_1713-45insTGT
ENST00000268124.11:c.1713-46_1713-45insTGT MANE Select ENSP00000268124.5:n.1713-46_1713-45insTGT
ENST00000530292.3:c.1314-46_1314-45insTGT ENSP00000432885.2:n.1314-46_1314-45insTGT
ENST00000635986.2:c.1713-46_1713-45insTGT ENSP00000490653.2:n.1713-46_1713-45insTGT
ENST00000636774.1:c.*280-46_*280-45insTGT ENSP00000489799.1:n.*280-46_*280-45insTGT
ENST00000637238.1:c.450-46_450-45insTGT ENSP00000490756.1:n.450-46_450-45insTGT
ENST00000637264.1:c.785-46_785-45insTGT
ENST00000666746.1:c.1290-46_1290-45insTGT
ENST00000670281.1:c.33-46_33-45insTGT ENSP00000499709.1:n.33-46_33-45insTGT
ENST00000672071.1:n.1911-46_1911-45insTGT
ENST00000672923.2:n.1816-46_1816-45insTGT
ENST00000268124.9:c.1713-46_1713-45insTGT ENSP00000268124.5:n.1713-46_1713-45insTGT
ENST00000442287.6:c.1713-46_1713-45insTGT ENSP00000399851.2:n.1713-46_1713-45insTGT
ENST00000526314.2:c.95-46_95-45insTGT
ENST00000631044.2:c.*1096-46_*1096-45insTGT ENSP00000486730.1:n.*1096-46_*1096-45insTGT
NM_001126131.1:c.1713-46_1713-45insTGT NP_001119603.1:n.1713-46_1713-45insTGT
NM_002693.2:c.1713-46_1713-45insTGT NP_002684.1:n.1713-46_1713-45insTGT
NM_001126131.2:c.1713-46_1713-45insTGT NP_001119603.1:n.1713-46_1713-45insTGT
NM_002693.3:c.1713-46_1713-45insTGT MANE Select NP_002684.1:n.1713-46_1713-45insTGT