Canonical Allele Identifier: CA2805170395

Gene: POLG

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.89325722_89325723insA , CM000677.2:g.89325722_89325723insA	GRCh38
NC_000015.9:g.89868953_89868954insA , CM000677.1:g.89868953_89868954insA	GRCh37
NC_000015.8:g.87669957_87669958insA	NCBI36
NG_008218.1:g.14073_14074insT
NG_008218.2:g.14073_14074insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000636937.2:c.1713-37_1713-36insT	ENSP00000516154.1:n.1713-37_1713-36insT
ENST00000268124.11:c.1713-37_1713-36insT MANE Select	ENSP00000268124.5:n.1713-37_1713-36insT
ENST00000530292.3:c.1314-37_1314-36insT	ENSP00000432885.2:n.1314-37_1314-36insT
ENST00000635986.2:c.1713-37_1713-36insT	ENSP00000490653.2:n.1713-37_1713-36insT
ENST00000636774.1:c.*280-37_*280-36insT	ENSP00000489799.1:n.*280-37_*280-36insT
ENST00000637238.1:c.450-37_450-36insT	ENSP00000490756.1:n.450-37_450-36insT
ENST00000637264.1:c.785-37_785-36insT
ENST00000666746.1:c.1290-37_1290-36insT
ENST00000670281.1:c.33-37_33-36insT	ENSP00000499709.1:n.33-37_33-36insT
ENST00000672071.1:n.1911-37_1911-36insT
ENST00000672923.2:n.1816-37_1816-36insT
ENST00000268124.9:c.1713-37_1713-36insT	ENSP00000268124.5:n.1713-37_1713-36insT
ENST00000442287.6:c.1713-37_1713-36insT	ENSP00000399851.2:n.1713-37_1713-36insT
ENST00000526314.2:c.95-37_95-36insT
ENST00000631044.2:c.*1096-37_*1096-36insT	ENSP00000486730.1:n.*1096-37_*1096-36insT
NM_001126131.1:c.1713-37_1713-36insT	NP_001119603.1:n.1713-37_1713-36insT
NM_002693.2:c.1713-37_1713-36insT	NP_002684.1:n.1713-37_1713-36insT
NM_001126131.2:c.1713-37_1713-36insT	NP_001119603.1:n.1713-37_1713-36insT
NM_002693.3:c.1713-37_1713-36insT MANE Select	NP_002684.1:n.1713-37_1713-36insT