Canonical Allele Identifier: CA2805170441
Gene: POLG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.89325750_89325751insAGA , CM000677.2:g.89325750_89325751insAGA GRCh38
NC_000015.9:g.89868981_89868982insAGA , CM000677.1:g.89868981_89868982insAGA GRCh37
NC_000015.8:g.87669985_87669986insAGA NCBI36
NG_008218.1:g.14045_14046insTCT
NG_008218.2:g.14045_14046insTCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000636937.2:c.1713-65_1713-64insTCT ENSP00000516154.1:n.1713-65_1713-64insTCT
ENST00000268124.11:c.1713-65_1713-64insTCT MANE Select ENSP00000268124.5:n.1713-65_1713-64insTCT
ENST00000530292.3:c.1314-65_1314-64insTCT ENSP00000432885.2:n.1314-65_1314-64insTCT
ENST00000635986.2:c.1713-65_1713-64insTCT ENSP00000490653.2:n.1713-65_1713-64insTCT
ENST00000636774.1:c.*280-65_*280-64insTCT ENSP00000489799.1:n.*280-65_*280-64insTCT
ENST00000637238.1:c.450-65_450-64insTCT ENSP00000490756.1:n.450-65_450-64insTCT
ENST00000637264.1:c.785-65_785-64insTCT
ENST00000666746.1:c.1290-65_1290-64insTCT
ENST00000670281.1:c.33-65_33-64insTCT ENSP00000499709.1:n.33-65_33-64insTCT
ENST00000672071.1:n.1911-65_1911-64insTCT
ENST00000672923.2:n.1816-65_1816-64insTCT
ENST00000268124.9:c.1713-65_1713-64insTCT ENSP00000268124.5:n.1713-65_1713-64insTCT
ENST00000442287.6:c.1713-65_1713-64insTCT ENSP00000399851.2:n.1713-65_1713-64insTCT
ENST00000526314.2:c.95-65_95-64insTCT
ENST00000631044.2:c.*1096-65_*1096-64insTCT ENSP00000486730.1:n.*1096-65_*1096-64insTCT
NM_001126131.1:c.1713-65_1713-64insTCT NP_001119603.1:n.1713-65_1713-64insTCT
NM_002693.2:c.1713-65_1713-64insTCT NP_002684.1:n.1713-65_1713-64insTCT
NM_001126131.2:c.1713-65_1713-64insTCT NP_001119603.1:n.1713-65_1713-64insTCT
NM_002693.3:c.1713-65_1713-64insTCT MANE Select NP_002684.1:n.1713-65_1713-64insTCT