Canonical Allele Identifier: CA2194547974
Gene: POLG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.89320919C= , CM000677.2:g.89320919C= GRCh38
NC_000015.9:g.89864150C= , CM000677.1:g.89864150C= GRCh37
NC_000015.8:g.87665154C= NCBI36
NG_008218.1:g.18877G=
NG_008218.2:g.18877G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000636937.2:c.2828G= ENSP00000516154.1:p.Arg943=
ENST00000268124.11:c.2828G= MANE Select ENSP00000268124.5:p.Arg943=
ENST00000530292.3:c.2429G= ENSP00000432885.2:p.Arg810=
ENST00000635986.2:c.2828G= ENSP00000490653.2:p.Arg943=
ENST00000636774.1:c.*1395G= ENSP00000489799.1:n.*1395G=
ENST00000637238.1:c.1637G= ENSP00000490756.1:n.1637G=
ENST00000637264.1:c.1900G=
ENST00000666746.1:c.2405G=
ENST00000670281.1:c.800+1043G= ENSP00000499709.1:n.800+1043G=
ENST00000672071.1:n.3026G=
ENST00000672695.1:n.5G=
ENST00000672923.2:n.2770G=
ENST00000268124.9:c.2828G= ENSP00000268124.5:p.Arg943=
ENST00000442287.6:c.2828G= ENSP00000399851.2:p.Arg943=
ENST00000528881.2:c.425G=
ENST00000530715.5:c.186-50G= ENSP00000431395.1:n.186-50G=
ENST00000631044.2:c.*2252G= ENSP00000486730.1:n.*2252G=
NM_001126131.1:c.2828G= NP_001119603.1:p.Arg943=
NM_002693.2:c.2828G= NP_002684.1:p.Arg943=
NM_001126131.2:c.2828G= NP_001119603.1:p.Arg943=
NM_002693.3:c.2828G= MANE Select NP_002684.1:p.Arg943=