Canonical Allele Identifier: CA2194555977
Gene: POLG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.89323622_89323624delinsATG , CM000677.2:g.89323622_89323624delinsATG GRCh38
NC_000015.9:g.89866853_89866855delinsATG , CM000677.1:g.89866853_89866855delinsATG GRCh37
NC_000015.8:g.87667857_87667859delinsATG NCBI36
NG_008218.1:g.16172_16174delinsCAT
NG_008218.2:g.16172_16174delinsCAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000636937.2:c.2158-113_2158-111delinsCAT ENSP00000516154.1:n.2158-113_2158-111delinsCAT
ENST00000268124.11:c.2158-113_2158-111delinsCAT MANE Select ENSP00000268124.5:n.2158-113_2158-111delinsCAT
ENST00000530292.3:c.1759-113_1759-111delinsCAT ENSP00000432885.2:n.1759-113_1759-111delinsCAT
ENST00000635986.2:c.2158-113_2158-111delinsCAT ENSP00000490653.2:n.2158-113_2158-111delinsCAT
ENST00000636774.1:c.*725-113_*725-111delinsCAT ENSP00000489799.1:n.*725-113_*725-111delinsCAT
ENST00000637238.1:c.855-113_855-111delinsCAT ENSP00000490756.1:n.855-113_855-111delinsCAT
ENST00000637264.1:c.1230-113_1230-111delinsCAT
ENST00000666746.1:c.1735-113_1735-111delinsCAT
ENST00000670281.1:c.478-113_478-111delinsCAT ENSP00000499709.1:n.478-113_478-111delinsCAT
ENST00000672071.1:n.2356-113_2356-111delinsCAT
ENST00000672923.2:n.2261-113_2261-111delinsCAT
ENST00000268124.9:c.2158-113_2158-111delinsCAT ENSP00000268124.5:n.2158-113_2158-111delinsCAT
ENST00000442287.6:c.2158-113_2158-111delinsCAT ENSP00000399851.2:n.2158-113_2158-111delinsCAT
ENST00000526314.2:c.539+191_539+193delinsCAT
ENST00000526398.1:c.307-113_307-111delinsCAT
ENST00000526573.1:n.434_436delinsCAT
ENST00000532584.5:n.360-113_360-111delinsCAT
ENST00000533857.1:n.463_465delinsCAT
ENST00000631044.2:c.*1541-72_*1541-70delinsCAT ENSP00000486730.1:n.*1541-72_*1541-70delinsCAT
NM_001126131.1:c.2158-113_2158-111delinsCAT NP_001119603.1:n.2158-113_2158-111delinsCAT
NM_002693.2:c.2158-113_2158-111delinsCAT NP_002684.1:n.2158-113_2158-111delinsCAT
NM_001126131.2:c.2158-113_2158-111delinsCAT NP_001119603.1:n.2158-113_2158-111delinsCAT
NM_002693.3:c.2158-113_2158-111delinsCAT MANE Select NP_002684.1:n.2158-113_2158-111delinsCAT