Canonical Allele Identifier: CA2194561647
Gene: POLG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.89328735G= , CM000677.2:g.89328735G= GRCh38
NC_000015.9:g.89871966G= , CM000677.1:g.89871966G= GRCh37
NC_000015.8:g.87672970G= NCBI36
NG_008218.1:g.11061C=
NG_008218.2:g.11061C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000636937.2:c.1120C= ENSP00000516154.1:p.Arg374=
ENST00000268124.11:c.1120C= MANE Select ENSP00000268124.5:p.Arg374=
ENST00000530292.3:c.721C= ENSP00000432885.2:p.Arg241=
ENST00000635986.2:c.1120C= ENSP00000490653.2:p.Arg374=
ENST00000636774.1:c.1120C= ENSP00000489799.1:p.Arg374=
ENST00000637264.1:c.192C=
ENST00000666746.1:c.777C=
ENST00000672071.1:n.1318C=
ENST00000672923.2:n.117C=
ENST00000268124.9:c.1120C= ENSP00000268124.5:p.Arg374=
ENST00000442287.6:c.1120C= ENSP00000399851.2:p.Arg374=
ENST00000631044.2:c.*503C= ENSP00000486730.1:n.*503C=
NM_001126131.1:c.1120C= NP_001119603.1:p.Arg374=
NM_002693.2:c.1120C= NP_002684.1:p.Arg374=
NM_001126131.2:c.1120C= NP_001119603.1:p.Arg374=
NM_002693.3:c.1120C= MANE Select NP_002684.1:p.Arg374=