Canonical Allele Identifier: CA2805169528
Gene: POLG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.89323603_89323604insA , CM000677.2:g.89323603_89323604insA GRCh38
NC_000015.9:g.89866834_89866835insA , CM000677.1:g.89866834_89866835insA GRCh37
NC_000015.8:g.87667838_87667839insA NCBI36
NG_008218.1:g.16192_16193insT
NG_008218.2:g.16192_16193insT

Transcript Alleles

HGVS Amino-acid Change
ENST00000636937.2:c.2158-93_2158-92insT ENSP00000516154.1:n.2158-93_2158-92insT
ENST00000268124.11:c.2158-93_2158-92insT MANE Select ENSP00000268124.5:n.2158-93_2158-92insT
ENST00000530292.3:c.1759-93_1759-92insT ENSP00000432885.2:n.1759-93_1759-92insT
ENST00000635986.2:c.2158-93_2158-92insT ENSP00000490653.2:n.2158-93_2158-92insT
ENST00000636774.1:c.*725-93_*725-92insT ENSP00000489799.1:n.*725-93_*725-92insT
ENST00000637238.1:c.855-93_855-92insT ENSP00000490756.1:n.855-93_855-92insT
ENST00000637264.1:c.1230-93_1230-92insT
ENST00000666746.1:c.1735-93_1735-92insT
ENST00000670281.1:c.478-93_478-92insT ENSP00000499709.1:n.478-93_478-92insT
ENST00000672071.1:n.2356-93_2356-92insT
ENST00000672923.2:n.2261-93_2261-92insT
ENST00000268124.9:c.2158-93_2158-92insT ENSP00000268124.5:n.2158-93_2158-92insT
ENST00000442287.6:c.2158-93_2158-92insT ENSP00000399851.2:n.2158-93_2158-92insT
ENST00000526314.2:c.539+211_539+212insT
ENST00000526398.1:c.307-93_307-92insT
ENST00000526573.1:n.454_455insT
ENST00000532584.5:n.360-93_360-92insT
ENST00000533857.1:n.483_484insT
ENST00000631044.2:c.*1541-52_*1541-51insT ENSP00000486730.1:n.*1541-52_*1541-51insT
NM_001126131.1:c.2158-93_2158-92insT NP_001119603.1:n.2158-93_2158-92insT
NM_002693.2:c.2158-93_2158-92insT NP_002684.1:n.2158-93_2158-92insT
NM_001126131.2:c.2158-93_2158-92insT NP_001119603.1:n.2158-93_2158-92insT
NM_002693.3:c.2158-93_2158-92insT MANE Select NP_002684.1:n.2158-93_2158-92insT