Canonical Allele Identifier: CA2805170460

Gene: POLG

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.89325762_89325763insACA , CM000677.2:g.89325762_89325763insACA	GRCh38
NC_000015.9:g.89868993_89868994insACA , CM000677.1:g.89868993_89868994insACA	GRCh37
NC_000015.8:g.87669997_87669998insACA	NCBI36
NG_008218.1:g.14033_14034insTGT
NG_008218.2:g.14033_14034insTGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000636937.2:c.1713-77_1713-76insTGT	ENSP00000516154.1:n.1713-77_1713-76insTGT
ENST00000268124.11:c.1713-77_1713-76insTGT MANE Select	ENSP00000268124.5:n.1713-77_1713-76insTGT
ENST00000530292.3:c.1314-77_1314-76insTGT	ENSP00000432885.2:n.1314-77_1314-76insTGT
ENST00000635986.2:c.1713-77_1713-76insTGT	ENSP00000490653.2:n.1713-77_1713-76insTGT
ENST00000636774.1:c.*280-77_*280-76insTGT	ENSP00000489799.1:n.*280-77_*280-76insTGT
ENST00000637238.1:c.450-77_450-76insTGT	ENSP00000490756.1:n.450-77_450-76insTGT
ENST00000637264.1:c.785-77_785-76insTGT
ENST00000666746.1:c.1290-77_1290-76insTGT
ENST00000670281.1:c.33-77_33-76insTGT	ENSP00000499709.1:n.33-77_33-76insTGT
ENST00000672071.1:n.1911-77_1911-76insTGT
ENST00000672923.2:n.1816-77_1816-76insTGT
ENST00000268124.9:c.1713-77_1713-76insTGT	ENSP00000268124.5:n.1713-77_1713-76insTGT
ENST00000442287.6:c.1713-77_1713-76insTGT	ENSP00000399851.2:n.1713-77_1713-76insTGT
ENST00000526314.2:c.95-77_95-76insTGT
ENST00000631044.2:c.*1096-77_*1096-76insTGT	ENSP00000486730.1:n.*1096-77_*1096-76insTGT
NM_001126131.1:c.1713-77_1713-76insTGT	NP_001119603.1:n.1713-77_1713-76insTGT
NM_002693.2:c.1713-77_1713-76insTGT	NP_002684.1:n.1713-77_1713-76insTGT
NM_001126131.2:c.1713-77_1713-76insTGT	NP_001119603.1:n.1713-77_1713-76insTGT
NM_002693.3:c.1713-77_1713-76insTGT MANE Select	NP_002684.1:n.1713-77_1713-76insTGT