Canonical Allele Identifier: CA2805169535

Gene: POLG

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.89323610_89323611insG , CM000677.2:g.89323610_89323611insG	GRCh38
NC_000015.9:g.89866841_89866842insG , CM000677.1:g.89866841_89866842insG	GRCh37
NC_000015.8:g.87667845_87667846insG	NCBI36
NG_008218.1:g.16185_16186insC
NG_008218.2:g.16185_16186insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000636937.2:c.2158-100_2158-99insC	ENSP00000516154.1:n.2158-100_2158-99insC
ENST00000268124.11:c.2158-100_2158-99insC MANE Select	ENSP00000268124.5:n.2158-100_2158-99insC
ENST00000530292.3:c.1759-100_1759-99insC	ENSP00000432885.2:n.1759-100_1759-99insC
ENST00000635986.2:c.2158-100_2158-99insC	ENSP00000490653.2:n.2158-100_2158-99insC
ENST00000636774.1:c.*725-100_*725-99insC	ENSP00000489799.1:n.*725-100_*725-99insC
ENST00000637238.1:c.855-100_855-99insC	ENSP00000490756.1:n.855-100_855-99insC
ENST00000637264.1:c.1230-100_1230-99insC
ENST00000666746.1:c.1735-100_1735-99insC
ENST00000670281.1:c.478-100_478-99insC	ENSP00000499709.1:n.478-100_478-99insC
ENST00000672071.1:n.2356-100_2356-99insC
ENST00000672923.2:n.2261-100_2261-99insC
ENST00000268124.9:c.2158-100_2158-99insC	ENSP00000268124.5:n.2158-100_2158-99insC
ENST00000442287.6:c.2158-100_2158-99insC	ENSP00000399851.2:n.2158-100_2158-99insC
ENST00000526314.2:c.539+204_539+205insC
ENST00000526398.1:c.307-100_307-99insC
ENST00000526573.1:n.447_448insC
ENST00000532584.5:n.360-100_360-99insC
ENST00000533857.1:n.476_477insC
ENST00000631044.2:c.*1541-59_*1541-58insC	ENSP00000486730.1:n.*1541-59_*1541-58insC
NM_001126131.1:c.2158-100_2158-99insC	NP_001119603.1:n.2158-100_2158-99insC
NM_002693.2:c.2158-100_2158-99insC	NP_002684.1:n.2158-100_2158-99insC
NM_001126131.2:c.2158-100_2158-99insC	NP_001119603.1:n.2158-100_2158-99insC
NM_002693.3:c.2158-100_2158-99insC MANE Select	NP_002684.1:n.2158-100_2158-99insC