Canonical Allele Identifier: CA2805170437
Gene: POLG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.89325749_89325750insACA , CM000677.2:g.89325749_89325750insACA GRCh38
NC_000015.9:g.89868980_89868981insACA , CM000677.1:g.89868980_89868981insACA GRCh37
NC_000015.8:g.87669984_87669985insACA NCBI36
NG_008218.1:g.14046_14047insTGT
NG_008218.2:g.14046_14047insTGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000636937.2:c.1713-64_1713-63insTGT ENSP00000516154.1:n.1713-64_1713-63insTGT
ENST00000268124.11:c.1713-64_1713-63insTGT MANE Select ENSP00000268124.5:n.1713-64_1713-63insTGT
ENST00000530292.3:c.1314-64_1314-63insTGT ENSP00000432885.2:n.1314-64_1314-63insTGT
ENST00000635986.2:c.1713-64_1713-63insTGT ENSP00000490653.2:n.1713-64_1713-63insTGT
ENST00000636774.1:c.*280-64_*280-63insTGT ENSP00000489799.1:n.*280-64_*280-63insTGT
ENST00000637238.1:c.450-64_450-63insTGT ENSP00000490756.1:n.450-64_450-63insTGT
ENST00000637264.1:c.785-64_785-63insTGT
ENST00000666746.1:c.1290-64_1290-63insTGT
ENST00000670281.1:c.33-64_33-63insTGT ENSP00000499709.1:n.33-64_33-63insTGT
ENST00000672071.1:n.1911-64_1911-63insTGT
ENST00000672923.2:n.1816-64_1816-63insTGT
ENST00000268124.9:c.1713-64_1713-63insTGT ENSP00000268124.5:n.1713-64_1713-63insTGT
ENST00000442287.6:c.1713-64_1713-63insTGT ENSP00000399851.2:n.1713-64_1713-63insTGT
ENST00000526314.2:c.95-64_95-63insTGT
ENST00000631044.2:c.*1096-64_*1096-63insTGT ENSP00000486730.1:n.*1096-64_*1096-63insTGT
NM_001126131.1:c.1713-64_1713-63insTGT NP_001119603.1:n.1713-64_1713-63insTGT
NM_002693.2:c.1713-64_1713-63insTGT NP_002684.1:n.1713-64_1713-63insTGT
NM_001126131.2:c.1713-64_1713-63insTGT NP_001119603.1:n.1713-64_1713-63insTGT
NM_002693.3:c.1713-64_1713-63insTGT MANE Select NP_002684.1:n.1713-64_1713-63insTGT