Canonical Allele Identifier: CA2194548675
Gene: POLG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.89321150T= , CM000677.2:g.89321150T= GRCh38
NC_000015.9:g.89864381T= , CM000677.1:g.89864381T= GRCh37
NC_000015.8:g.87665385T= NCBI36
NG_008218.1:g.18646A=
NG_008218.2:g.18646A=

Transcript Alleles

HGVS Amino-acid change
ENST00000636937.2:c.2709A= ENSP00000516154.1:p.Gly903=
ENST00000268124.11:c.2709A= MANE Select ENSP00000268124.5:p.Gly903=
ENST00000530292.3:c.2310A= ENSP00000432885.2:p.Gly770=
ENST00000635986.2:c.2709A= ENSP00000490653.2:p.Gly903=
ENST00000636774.1:c.*1276A= ENSP00000489799.1:n.*1276A=
ENST00000637238.1:c.1406A= ENSP00000490756.1:n.1406A=
ENST00000637264.1:c.1781A=
ENST00000666746.1:c.2286A=
ENST00000670281.1:c.800+812A= ENSP00000499709.1:n.800+812A=
ENST00000672071.1:n.2907A=
ENST00000672923.2:n.2651A=
ENST00000268124.9:c.2709A= ENSP00000268124.5:p.Gly903=
ENST00000442287.6:c.2709A= ENSP00000399851.2:p.Gly903=
ENST00000528881.2:c.306A=
ENST00000530715.5:c.186-281A= ENSP00000431395.1:n.186-281A=
ENST00000631044.2:c.*2133A= ENSP00000486730.1:n.*2133A=
NM_001126131.1:c.2709A= NP_001119603.1:p.Gly903=
NM_002693.2:c.2709A= NP_002684.1:p.Gly903=
NM_001126131.2:c.2709A= NP_001119603.1:p.Gly903=
NM_002693.3:c.2709A= MANE Select NP_002684.1:p.Gly903=