Canonical Allele Identifier: CA2805170424

Gene: POLG

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.89325745_89325746insAC , CM000677.2:g.89325745_89325746insAC	GRCh38
NC_000015.9:g.89868976_89868977insAC , CM000677.1:g.89868976_89868977insAC	GRCh37
NC_000015.8:g.87669980_87669981insAC	NCBI36
NG_008218.1:g.14050_14051insGT
NG_008218.2:g.14050_14051insGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000636937.2:c.1713-60_1713-59insGT	ENSP00000516154.1:n.1713-60_1713-59insGT
ENST00000268124.11:c.1713-60_1713-59insGT MANE Select	ENSP00000268124.5:n.1713-60_1713-59insGT
ENST00000530292.3:c.1314-60_1314-59insGT	ENSP00000432885.2:n.1314-60_1314-59insGT
ENST00000635986.2:c.1713-60_1713-59insGT	ENSP00000490653.2:n.1713-60_1713-59insGT
ENST00000636774.1:c.*280-60_*280-59insGT	ENSP00000489799.1:n.*280-60_*280-59insGT
ENST00000637238.1:c.450-60_450-59insGT	ENSP00000490756.1:n.450-60_450-59insGT
ENST00000637264.1:c.785-60_785-59insGT
ENST00000666746.1:c.1290-60_1290-59insGT
ENST00000670281.1:c.33-60_33-59insGT	ENSP00000499709.1:n.33-60_33-59insGT
ENST00000672071.1:n.1911-60_1911-59insGT
ENST00000672923.2:n.1816-60_1816-59insGT
ENST00000268124.9:c.1713-60_1713-59insGT	ENSP00000268124.5:n.1713-60_1713-59insGT
ENST00000442287.6:c.1713-60_1713-59insGT	ENSP00000399851.2:n.1713-60_1713-59insGT
ENST00000526314.2:c.95-60_95-59insGT
ENST00000631044.2:c.*1096-60_*1096-59insGT	ENSP00000486730.1:n.*1096-60_*1096-59insGT
NM_001126131.1:c.1713-60_1713-59insGT	NP_001119603.1:n.1713-60_1713-59insGT
NM_002693.2:c.1713-60_1713-59insGT	NP_002684.1:n.1713-60_1713-59insGT
NM_001126131.2:c.1713-60_1713-59insGT	NP_001119603.1:n.1713-60_1713-59insGT
NM_002693.3:c.1713-60_1713-59insGT MANE Select	NP_002684.1:n.1713-60_1713-59insGT