Canonical Allele Identifier: CA2805170428

Gene: POLG

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.89325746_89325747insAGA , CM000677.2:g.89325746_89325747insAGA	GRCh38
NC_000015.9:g.89868977_89868978insAGA , CM000677.1:g.89868977_89868978insAGA	GRCh37
NC_000015.8:g.87669981_87669982insAGA	NCBI36
NG_008218.1:g.14049_14050insTCT
NG_008218.2:g.14049_14050insTCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000636937.2:c.1713-61_1713-60insTCT	ENSP00000516154.1:n.1713-61_1713-60insTCT
ENST00000268124.11:c.1713-61_1713-60insTCT MANE Select	ENSP00000268124.5:n.1713-61_1713-60insTCT
ENST00000530292.3:c.1314-61_1314-60insTCT	ENSP00000432885.2:n.1314-61_1314-60insTCT
ENST00000635986.2:c.1713-61_1713-60insTCT	ENSP00000490653.2:n.1713-61_1713-60insTCT
ENST00000636774.1:c.*280-61_*280-60insTCT	ENSP00000489799.1:n.*280-61_*280-60insTCT
ENST00000637238.1:c.450-61_450-60insTCT	ENSP00000490756.1:n.450-61_450-60insTCT
ENST00000637264.1:c.785-61_785-60insTCT
ENST00000666746.1:c.1290-61_1290-60insTCT
ENST00000670281.1:c.33-61_33-60insTCT	ENSP00000499709.1:n.33-61_33-60insTCT
ENST00000672071.1:n.1911-61_1911-60insTCT
ENST00000672923.2:n.1816-61_1816-60insTCT
ENST00000268124.9:c.1713-61_1713-60insTCT	ENSP00000268124.5:n.1713-61_1713-60insTCT
ENST00000442287.6:c.1713-61_1713-60insTCT	ENSP00000399851.2:n.1713-61_1713-60insTCT
ENST00000526314.2:c.95-61_95-60insTCT
ENST00000631044.2:c.*1096-61_*1096-60insTCT	ENSP00000486730.1:n.*1096-61_*1096-60insTCT
NM_001126131.1:c.1713-61_1713-60insTCT	NP_001119603.1:n.1713-61_1713-60insTCT
NM_002693.2:c.1713-61_1713-60insTCT	NP_002684.1:n.1713-61_1713-60insTCT
NM_001126131.2:c.1713-61_1713-60insTCT	NP_001119603.1:n.1713-61_1713-60insTCT
NM_002693.3:c.1713-61_1713-60insTCT MANE Select	NP_002684.1:n.1713-61_1713-60insTCT