Canonical Allele Identifier: CA2805170419

Gene: POLG

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.89325740_89325741insACA , CM000677.2:g.89325740_89325741insACA	GRCh38
NC_000015.9:g.89868971_89868972insACA , CM000677.1:g.89868971_89868972insACA	GRCh37
NC_000015.8:g.87669975_87669976insACA	NCBI36
NG_008218.1:g.14055_14056insTGT
NG_008218.2:g.14055_14056insTGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000636937.2:c.1713-55_1713-54insTGT	ENSP00000516154.1:n.1713-55_1713-54insTGT
ENST00000268124.11:c.1713-55_1713-54insTGT MANE Select	ENSP00000268124.5:n.1713-55_1713-54insTGT
ENST00000530292.3:c.1314-55_1314-54insTGT	ENSP00000432885.2:n.1314-55_1314-54insTGT
ENST00000635986.2:c.1713-55_1713-54insTGT	ENSP00000490653.2:n.1713-55_1713-54insTGT
ENST00000636774.1:c.*280-55_*280-54insTGT	ENSP00000489799.1:n.*280-55_*280-54insTGT
ENST00000637238.1:c.450-55_450-54insTGT	ENSP00000490756.1:n.450-55_450-54insTGT
ENST00000637264.1:c.785-55_785-54insTGT
ENST00000666746.1:c.1290-55_1290-54insTGT
ENST00000670281.1:c.33-55_33-54insTGT	ENSP00000499709.1:n.33-55_33-54insTGT
ENST00000672071.1:n.1911-55_1911-54insTGT
ENST00000672923.2:n.1816-55_1816-54insTGT
ENST00000268124.9:c.1713-55_1713-54insTGT	ENSP00000268124.5:n.1713-55_1713-54insTGT
ENST00000442287.6:c.1713-55_1713-54insTGT	ENSP00000399851.2:n.1713-55_1713-54insTGT
ENST00000526314.2:c.95-55_95-54insTGT
ENST00000631044.2:c.*1096-55_*1096-54insTGT	ENSP00000486730.1:n.*1096-55_*1096-54insTGT
NM_001126131.1:c.1713-55_1713-54insTGT	NP_001119603.1:n.1713-55_1713-54insTGT
NM_002693.2:c.1713-55_1713-54insTGT	NP_002684.1:n.1713-55_1713-54insTGT
NM_001126131.2:c.1713-55_1713-54insTGT	NP_001119603.1:n.1713-55_1713-54insTGT
NM_002693.3:c.1713-55_1713-54insTGT MANE Select	NP_002684.1:n.1713-55_1713-54insTGT