Canonical Allele Identifier: CA2194550142
Gene: POLG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.89321675G= , CM000677.2:g.89321675G= GRCh38
NC_000015.9:g.89864906G= , CM000677.1:g.89864906G= GRCh37
NC_000015.8:g.87665910G= NCBI36
NG_008218.1:g.18121C=
NG_008218.2:g.18121C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000636937.2:c.2598+61C= ENSP00000516154.1:n.2598+61C=
ENST00000268124.11:c.2598+61C= MANE Select ENSP00000268124.5:n.2598+61C=
ENST00000530292.3:c.2199+61C= ENSP00000432885.2:n.2199+61C=
ENST00000635986.2:c.2598+61C= ENSP00000490653.2:n.2598+61C=
ENST00000636774.1:c.*1165+61C= ENSP00000489799.1:n.*1165+61C=
ENST00000637238.1:c.1295+61C= ENSP00000490756.1:n.1295+61C=
ENST00000637264.1:c.1670+61C=
ENST00000666746.1:c.2175+61C=
ENST00000670281.1:c.800+287C= ENSP00000499709.1:n.800+287C=
ENST00000672071.1:n.2796+61C=
ENST00000672923.2:n.2540+61C=
ENST00000268124.9:c.2598+61C= ENSP00000268124.5:n.2598+61C=
ENST00000442287.6:c.2598+61C= ENSP00000399851.2:n.2598+61C=
ENST00000528881.2:c.196-415C=
ENST00000530715.5:c.186-806C= ENSP00000431395.1:n.186-806C=
ENST00000631044.2:c.*2022+61C= ENSP00000486730.1:n.*2022+61C=
NM_001126131.1:c.2598+61C= NP_001119603.1:n.2598+61C=
NM_002693.2:c.2598+61C= NP_002684.1:n.2598+61C=
NM_001126131.2:c.2598+61C= NP_001119603.1:n.2598+61C=
NM_002693.3:c.2598+61C= MANE Select NP_002684.1:n.2598+61C=