Canonical Allele Identifier: CA2194550567
Gene: POLG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.89321785A= , CM000677.2:g.89321785A= GRCh38
NC_000015.9:g.89865016A= , CM000677.1:g.89865016A= GRCh37
NC_000015.8:g.87666020A= NCBI36
NG_008218.1:g.18011T=
NG_008218.2:g.18011T=

Transcript Alleles

HGVS Amino-acid change
ENST00000636937.2:c.2549T= ENSP00000516154.1:p.Ile850=
ENST00000268124.11:c.2549T= MANE Select ENSP00000268124.5:p.Ile850=
ENST00000530292.3:c.2150T= ENSP00000432885.2:p.Ile717=
ENST00000635986.2:c.2549T= ENSP00000490653.2:p.Ile850=
ENST00000636774.1:c.*1116T= ENSP00000489799.1:n.*1116T=
ENST00000637238.1:c.1246T= ENSP00000490756.1:n.1246T=
ENST00000637264.1:c.1621T=
ENST00000666746.1:c.2126T=
ENST00000670281.1:c.800+177T= ENSP00000499709.1:n.800+177T=
ENST00000672071.1:n.2747T=
ENST00000672923.2:n.2491T=
ENST00000268124.9:c.2549T= ENSP00000268124.5:p.Ile850=
ENST00000442287.6:c.2549T= ENSP00000399851.2:p.Ile850=
ENST00000528881.2:c.196-525T=
ENST00000530715.5:c.186-916T= ENSP00000431395.1:n.186-916T=
ENST00000532584.5:n.698T=
ENST00000631044.2:c.*1973T= ENSP00000486730.1:n.*1973T=
NM_001126131.1:c.2549T= NP_001119603.1:p.Ile850=
NM_002693.2:c.2549T= NP_002684.1:p.Ile850=
NM_001126131.2:c.2549T= NP_001119603.1:p.Ile850=
NM_002693.3:c.2549T= MANE Select NP_002684.1:p.Ile850=