Canonical Allele Identifier: CA2805170393
Gene: POLG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.89325717_89325718insAGA , CM000677.2:g.89325717_89325718insAGA GRCh38
NC_000015.9:g.89868948_89868949insAGA , CM000677.1:g.89868948_89868949insAGA GRCh37
NC_000015.8:g.87669952_87669953insAGA NCBI36
NG_008218.1:g.14078_14079insTCT
NG_008218.2:g.14078_14079insTCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000636937.2:c.1713-32_1713-31insTCT ENSP00000516154.1:n.1713-32_1713-31insTCT
ENST00000268124.11:c.1713-32_1713-31insTCT MANE Select ENSP00000268124.5:n.1713-32_1713-31insTCT
ENST00000530292.3:c.1314-32_1314-31insTCT ENSP00000432885.2:n.1314-32_1314-31insTCT
ENST00000635986.2:c.1713-32_1713-31insTCT ENSP00000490653.2:n.1713-32_1713-31insTCT
ENST00000636774.1:c.*280-32_*280-31insTCT ENSP00000489799.1:n.*280-32_*280-31insTCT
ENST00000637238.1:c.450-32_450-31insTCT ENSP00000490756.1:n.450-32_450-31insTCT
ENST00000637264.1:c.785-32_785-31insTCT
ENST00000666746.1:c.1290-32_1290-31insTCT
ENST00000670281.1:c.33-32_33-31insTCT ENSP00000499709.1:n.33-32_33-31insTCT
ENST00000672071.1:n.1911-32_1911-31insTCT
ENST00000672923.2:n.1816-32_1816-31insTCT
ENST00000268124.9:c.1713-32_1713-31insTCT ENSP00000268124.5:n.1713-32_1713-31insTCT
ENST00000442287.6:c.1713-32_1713-31insTCT ENSP00000399851.2:n.1713-32_1713-31insTCT
ENST00000526314.2:c.95-32_95-31insTCT
ENST00000631044.2:c.*1096-32_*1096-31insTCT ENSP00000486730.1:n.*1096-32_*1096-31insTCT
NM_001126131.1:c.1713-32_1713-31insTCT NP_001119603.1:n.1713-32_1713-31insTCT
NM_002693.2:c.1713-32_1713-31insTCT NP_002684.1:n.1713-32_1713-31insTCT
NM_001126131.2:c.1713-32_1713-31insTCT NP_001119603.1:n.1713-32_1713-31insTCT
NM_002693.3:c.1713-32_1713-31insTCT MANE Select NP_002684.1:n.1713-32_1713-31insTCT