Canonical Allele Identifier: CA2805170381

Gene: POLG

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.89325690_89325691insACA , CM000677.2:g.89325690_89325691insACA	GRCh38
NC_000015.9:g.89868921_89868922insACA , CM000677.1:g.89868921_89868922insACA	GRCh37
NC_000015.8:g.87669925_87669926insACA	NCBI36
NG_008218.1:g.14105_14106insTGT
NG_008218.2:g.14105_14106insTGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000636937.2:c.1713-5_1713-4insTGT	ENSP00000516154.1:n.1713-5_1713-4insTGT
ENST00000268124.11:c.1713-5_1713-4insTGT MANE Select	ENSP00000268124.5:n.1713-5_1713-4insTGT
ENST00000530292.3:c.1314-5_1314-4insTGT	ENSP00000432885.2:n.1314-5_1314-4insTGT
ENST00000635986.2:c.1713-5_1713-4insTGT	ENSP00000490653.2:n.1713-5_1713-4insTGT
ENST00000636774.1:c.*280-5_*280-4insTGT	ENSP00000489799.1:n.*280-5_*280-4insTGT
ENST00000637238.1:c.450-5_450-4insTGT	ENSP00000490756.1:n.450-5_450-4insTGT
ENST00000637264.1:c.785-5_785-4insTGT
ENST00000666746.1:c.1290-5_1290-4insTGT
ENST00000670281.1:c.33-5_33-4insTGT	ENSP00000499709.1:n.33-5_33-4insTGT
ENST00000672071.1:n.1911-5_1911-4insTGT
ENST00000672923.2:n.1816-5_1816-4insTGT
ENST00000268124.9:c.1713-5_1713-4insTGT	ENSP00000268124.5:n.1713-5_1713-4insTGT
ENST00000442287.6:c.1713-5_1713-4insTGT	ENSP00000399851.2:n.1713-5_1713-4insTGT
ENST00000526314.2:c.95-5_95-4insTGT
ENST00000631044.2:c.*1096-5_*1096-4insTGT	ENSP00000486730.1:n.*1096-5_*1096-4insTGT
NM_001126131.1:c.1713-5_1713-4insTGT	NP_001119603.1:n.1713-5_1713-4insTGT
NM_002693.2:c.1713-5_1713-4insTGT	NP_002684.1:n.1713-5_1713-4insTGT
NM_001126131.2:c.1713-5_1713-4insTGT	NP_001119603.1:n.1713-5_1713-4insTGT
NM_002693.3:c.1713-5_1713-4insTGT MANE Select	NP_002684.1:n.1713-5_1713-4insTGT