Canonical Allele Identifier: CA2194555725
Gene: POLG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.89323528C= , CM000677.2:g.89323528C= GRCh38
NC_000015.9:g.89866759C= , CM000677.1:g.89866759C= GRCh37
NC_000015.8:g.87667763C= NCBI36
NG_008218.1:g.16268G=
NG_008218.2:g.16268G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000636937.2:c.2158-17G= ENSP00000516154.1:n.2158-17G=
ENST00000268124.11:c.2158-17G= MANE Select ENSP00000268124.5:n.2158-17G=
ENST00000530292.3:c.1759-17G= ENSP00000432885.2:n.1759-17G=
ENST00000635986.2:c.2158-17G= ENSP00000490653.2:n.2158-17G=
ENST00000636774.1:c.*725-17G= ENSP00000489799.1:n.*725-17G=
ENST00000637238.1:c.855-17G= ENSP00000490756.1:n.855-17G=
ENST00000637264.1:c.1230-17G=
ENST00000666746.1:c.1735-17G=
ENST00000670281.1:c.478-17G= ENSP00000499709.1:n.478-17G=
ENST00000672071.1:n.2356-17G=
ENST00000672923.2:n.2261-17G=
ENST00000268124.9:c.2158-17G= ENSP00000268124.5:n.2158-17G=
ENST00000442287.6:c.2158-17G= ENSP00000399851.2:n.2158-17G=
ENST00000526314.2:c.539+287G=
ENST00000526398.1:c.307-17G=
ENST00000526573.1:n.530G=
ENST00000532584.5:n.360-17G=
ENST00000533857.1:n.559G=
ENST00000631044.2:c.*1565G= ENSP00000486730.1:n.*1565G=
NM_001126131.1:c.2158-17G= NP_001119603.1:n.2158-17G=
NM_002693.2:c.2158-17G= NP_002684.1:n.2158-17G=
NM_001126131.2:c.2158-17G= NP_001119603.1:n.2158-17G=
NM_002693.3:c.2158-17G= MANE Select NP_002684.1:n.2158-17G=