Canonical Allele Identifier: CA2194547903
Gene: POLG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.89320907T= , CM000677.2:g.89320907T= GRCh38
NC_000015.9:g.89864138T= , CM000677.1:g.89864138T= GRCh37
NC_000015.8:g.87665142T= NCBI36
NG_008218.1:g.18889A=
NG_008218.2:g.18889A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000636937.2:c.2840A= ENSP00000516154.1:p.Lys947=
ENST00000268124.11:c.2840A= MANE Select ENSP00000268124.5:p.Lys947=
ENST00000530292.3:c.2441A= ENSP00000432885.2:p.Lys814=
ENST00000635986.2:c.2840A= ENSP00000490653.2:p.Lys947=
ENST00000636774.1:c.*1407A= ENSP00000489799.1:n.*1407A=
ENST00000637238.1:c.1649A= ENSP00000490756.1:n.1649A=
ENST00000637264.1:c.1912A=
ENST00000666746.1:c.2417A=
ENST00000670281.1:c.800+1055A= ENSP00000499709.1:n.800+1055A=
ENST00000672071.1:n.3038A=
ENST00000672695.1:n.17A=
ENST00000672923.2:n.2782A=
ENST00000268124.9:c.2840A= ENSP00000268124.5:p.Lys947=
ENST00000442287.6:c.2840A= ENSP00000399851.2:p.Lys947=
ENST00000528881.2:c.437A=
ENST00000530715.5:c.186-38A= ENSP00000431395.1:n.186-38A=
ENST00000631044.2:c.*2264A= ENSP00000486730.1:n.*2264A=
NM_001126131.1:c.2840A= NP_001119603.1:p.Lys947=
NM_002693.2:c.2840A= NP_002684.1:p.Lys947=
NM_001126131.2:c.2840A= NP_001119603.1:p.Lys947=
NM_002693.3:c.2840A= MANE Select NP_002684.1:p.Lys947=