Canonical Allele Identifier: CA2194565368
Gene: POLG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.89330184G= , CM000677.2:g.89330184G= GRCh38
NC_000015.9:g.89873415G= , CM000677.1:g.89873415G= GRCh37
NC_000015.8:g.87674419G= NCBI36
NG_008218.1:g.9612C=
NG_008218.2:g.9612C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000636937.2:c.752C= ENSP00000516154.1:p.Thr251=
ENST00000268124.11:c.752C= MANE Select ENSP00000268124.5:p.Thr251=
ENST00000530292.3:c.353C= ENSP00000432885.2:p.Thr118=
ENST00000635986.2:c.752C= ENSP00000490653.2:p.Thr251=
ENST00000636774.1:c.752C= ENSP00000489799.1:p.Thr251=
ENST00000666746.1:c.409C=
ENST00000672071.1:n.950C=
ENST00000268124.9:c.752C= ENSP00000268124.5:p.Thr251=
ENST00000442287.6:c.752C= ENSP00000399851.2:p.Thr251=
ENST00000631044.2:c.*135C= ENSP00000486730.1:n.*135C=
NM_001126131.1:c.752C= NP_001119603.1:p.Thr251=
NM_002693.2:c.752C= NP_002684.1:p.Thr251=
NM_001126131.2:c.752C= NP_001119603.1:p.Thr251=
NM_002693.3:c.752C= MANE Select NP_002684.1:p.Thr251=