Canonical Allele Identifier: CA2805169510

Gene: POLG

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.89323539_89323540insACA , CM000677.2:g.89323539_89323540insACA	GRCh38
NC_000015.9:g.89866770_89866771insACA , CM000677.1:g.89866770_89866771insACA	GRCh37
NC_000015.8:g.87667774_87667775insACA	NCBI36
NG_008218.1:g.16256_16257insTGT
NG_008218.2:g.16256_16257insTGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000636937.2:c.2158-29_2158-28insTGT	ENSP00000516154.1:n.2158-29_2158-28insTGT
ENST00000268124.11:c.2158-29_2158-28insTGT MANE Select	ENSP00000268124.5:n.2158-29_2158-28insTGT
ENST00000530292.3:c.1759-29_1759-28insTGT	ENSP00000432885.2:n.1759-29_1759-28insTGT
ENST00000635986.2:c.2158-29_2158-28insTGT	ENSP00000490653.2:n.2158-29_2158-28insTGT
ENST00000636774.1:c.*725-29_*725-28insTGT	ENSP00000489799.1:n.*725-29_*725-28insTGT
ENST00000637238.1:c.855-29_855-28insTGT	ENSP00000490756.1:n.855-29_855-28insTGT
ENST00000637264.1:c.1230-29_1230-28insTGT
ENST00000666746.1:c.1735-29_1735-28insTGT
ENST00000670281.1:c.478-29_478-28insTGT	ENSP00000499709.1:n.478-29_478-28insTGT
ENST00000672071.1:n.2356-29_2356-28insTGT
ENST00000672923.2:n.2261-29_2261-28insTGT
ENST00000268124.9:c.2158-29_2158-28insTGT	ENSP00000268124.5:n.2158-29_2158-28insTGT
ENST00000442287.6:c.2158-29_2158-28insTGT	ENSP00000399851.2:n.2158-29_2158-28insTGT
ENST00000526314.2:c.539+275_539+276insTGT
ENST00000526398.1:c.307-29_307-28insTGT
ENST00000526573.1:n.518_519insTGT
ENST00000532584.5:n.360-29_360-28insTGT
ENST00000533857.1:n.547_548insTGT
ENST00000631044.2:c.*1553_*1554insTGT	ENSP00000486730.1:n.*1553_*1554insTGT
NM_001126131.1:c.2158-29_2158-28insTGT	NP_001119603.1:n.2158-29_2158-28insTGT
NM_002693.2:c.2158-29_2158-28insTGT	NP_002684.1:n.2158-29_2158-28insTGT
NM_001126131.2:c.2158-29_2158-28insTGT	NP_001119603.1:n.2158-29_2158-28insTGT
NM_002693.3:c.2158-29_2158-28insTGT MANE Select	NP_002684.1:n.2158-29_2158-28insTGT