Canonical Allele Identifier: CA2194550052
Gene: POLG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.89321648C= , CM000677.2:g.89321648C= GRCh38
NC_000015.9:g.89864879C= , CM000677.1:g.89864879C= GRCh37
NC_000015.8:g.87665883C= NCBI36
NG_008218.1:g.18148G=
NG_008218.2:g.18148G=

Transcript Alleles

HGVS Amino-acid change
ENST00000636937.2:c.2598+88G= ENSP00000516154.1:n.2598+88G=
ENST00000268124.11:c.2598+88G= MANE Select ENSP00000268124.5:n.2598+88G=
ENST00000530292.3:c.2199+88G= ENSP00000432885.2:n.2199+88G=
ENST00000635986.2:c.2598+88G= ENSP00000490653.2:n.2598+88G=
ENST00000636774.1:c.*1165+88G= ENSP00000489799.1:n.*1165+88G=
ENST00000637238.1:c.1295+88G= ENSP00000490756.1:n.1295+88G=
ENST00000637264.1:c.1670+88G=
ENST00000666746.1:c.2175+88G=
ENST00000670281.1:c.800+314G= ENSP00000499709.1:n.800+314G=
ENST00000672071.1:n.2796+88G=
ENST00000672923.2:n.2540+88G=
ENST00000268124.9:c.2598+88G= ENSP00000268124.5:n.2598+88G=
ENST00000442287.6:c.2598+88G= ENSP00000399851.2:n.2598+88G=
ENST00000528881.2:c.196-388G=
ENST00000530715.5:c.186-779G= ENSP00000431395.1:n.186-779G=
ENST00000631044.2:c.*2022+88G= ENSP00000486730.1:n.*2022+88G=
NM_001126131.1:c.2598+88G= NP_001119603.1:n.2598+88G=
NM_002693.2:c.2598+88G= NP_002684.1:n.2598+88G=
NM_001126131.2:c.2598+88G= NP_001119603.1:n.2598+88G=
NM_002693.3:c.2598+88G= MANE Select NP_002684.1:n.2598+88G=