Canonical Allele Identifier: CA2805170469

Gene: POLG

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.89325766_89325767insA , CM000677.2:g.89325766_89325767insA	GRCh38
NC_000015.9:g.89868997_89868998insA , CM000677.1:g.89868997_89868998insA	GRCh37
NC_000015.8:g.87670001_87670002insA	NCBI36
NG_008218.1:g.14029_14030insT
NG_008218.2:g.14029_14030insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000636937.2:c.1713-81_1713-80insT	ENSP00000516154.1:n.1713-81_1713-80insT
ENST00000268124.11:c.1713-81_1713-80insT MANE Select	ENSP00000268124.5:n.1713-81_1713-80insT
ENST00000530292.3:c.1314-81_1314-80insT	ENSP00000432885.2:n.1314-81_1314-80insT
ENST00000635986.2:c.1713-81_1713-80insT	ENSP00000490653.2:n.1713-81_1713-80insT
ENST00000636774.1:c.*280-81_*280-80insT	ENSP00000489799.1:n.*280-81_*280-80insT
ENST00000637238.1:c.450-81_450-80insT	ENSP00000490756.1:n.450-81_450-80insT
ENST00000637264.1:c.785-81_785-80insT
ENST00000666746.1:c.1290-81_1290-80insT
ENST00000670281.1:c.33-81_33-80insT	ENSP00000499709.1:n.33-81_33-80insT
ENST00000672071.1:n.1911-81_1911-80insT
ENST00000672923.2:n.1816-81_1816-80insT
ENST00000268124.9:c.1713-81_1713-80insT	ENSP00000268124.5:n.1713-81_1713-80insT
ENST00000442287.6:c.1713-81_1713-80insT	ENSP00000399851.2:n.1713-81_1713-80insT
ENST00000526314.2:c.95-81_95-80insT
ENST00000631044.2:c.*1096-81_*1096-80insT	ENSP00000486730.1:n.*1096-81_*1096-80insT
NM_001126131.1:c.1713-81_1713-80insT	NP_001119603.1:n.1713-81_1713-80insT
NM_002693.2:c.1713-81_1713-80insT	NP_002684.1:n.1713-81_1713-80insT
NM_001126131.2:c.1713-81_1713-80insT	NP_001119603.1:n.1713-81_1713-80insT
NM_002693.3:c.1713-81_1713-80insT MANE Select	NP_002684.1:n.1713-81_1713-80insT