Canonical Allele Identifier: CA2805170464
Gene: POLG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.89325763_89325764insA , CM000677.2:g.89325763_89325764insA GRCh38
NC_000015.9:g.89868994_89868995insA , CM000677.1:g.89868994_89868995insA GRCh37
NC_000015.8:g.87669998_87669999insA NCBI36
NG_008218.1:g.14032_14033insT
NG_008218.2:g.14032_14033insT

Transcript Alleles

HGVS Amino-acid Change
ENST00000636937.2:c.1713-78_1713-77insT ENSP00000516154.1:n.1713-78_1713-77insT
ENST00000268124.11:c.1713-78_1713-77insT MANE Select ENSP00000268124.5:n.1713-78_1713-77insT
ENST00000530292.3:c.1314-78_1314-77insT ENSP00000432885.2:n.1314-78_1314-77insT
ENST00000635986.2:c.1713-78_1713-77insT ENSP00000490653.2:n.1713-78_1713-77insT
ENST00000636774.1:c.*280-78_*280-77insT ENSP00000489799.1:n.*280-78_*280-77insT
ENST00000637238.1:c.450-78_450-77insT ENSP00000490756.1:n.450-78_450-77insT
ENST00000637264.1:c.785-78_785-77insT
ENST00000666746.1:c.1290-78_1290-77insT
ENST00000670281.1:c.33-78_33-77insT ENSP00000499709.1:n.33-78_33-77insT
ENST00000672071.1:n.1911-78_1911-77insT
ENST00000672923.2:n.1816-78_1816-77insT
ENST00000268124.9:c.1713-78_1713-77insT ENSP00000268124.5:n.1713-78_1713-77insT
ENST00000442287.6:c.1713-78_1713-77insT ENSP00000399851.2:n.1713-78_1713-77insT
ENST00000526314.2:c.95-78_95-77insT
ENST00000631044.2:c.*1096-78_*1096-77insT ENSP00000486730.1:n.*1096-78_*1096-77insT
NM_001126131.1:c.1713-78_1713-77insT NP_001119603.1:n.1713-78_1713-77insT
NM_002693.2:c.1713-78_1713-77insT NP_002684.1:n.1713-78_1713-77insT
NM_001126131.2:c.1713-78_1713-77insT NP_001119603.1:n.1713-78_1713-77insT
NM_002693.3:c.1713-78_1713-77insT MANE Select NP_002684.1:n.1713-78_1713-77insT