Canonical Allele Identifier: CA393751207
Gene: POLG HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.89319089T>G , CM000677.2:g.89319089T>G GRCh38
NC_000015.9:g.89862320T>G , CM000677.1:g.89862320T>G GRCh37
NC_000015.8:g.87663324T>G NCBI36
NG_008218.1:g.20707A>C
NG_011736.1:g.80127T>G , LRG_500:g.80127T>G
NG_008218.2:g.20707A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000636937.2:c.3115A>C ENSP00000516154.1:p.Lys1039Gln
ENST00000268124.11:c.3115A>C MANE Select ENSP00000268124.5:p.Lys1039Gln
ENST00000530292.3:c.2716A>C ENSP00000432885.2:p.Lys906Gln
ENST00000635986.2:c.*185A>C ENSP00000490653.2:n.*185A>C
ENST00000636530.1:n.75A>C
ENST00000636774.1:c.*1682A>C ENSP00000489799.1:n.*1682A>C
ENST00000637238.1:c.1924A>C ENSP00000490756.1:n.1924A>C
ENST00000637264.1:c.2187A>C
ENST00000666746.1:c.2692A>C
ENST00000672071.1:n.3313A>C
ENST00000672695.1:n.292A>C
ENST00000672923.2:n.3115A>C
ENST00000268124.9:c.3115A>C ENSP00000268124.5:p.Lys1039Gln
ENST00000442287.6:c.3115A>C ENSP00000399851.2:p.Lys1039Gln
ENST00000530292.2:c.199A>C ENSP00000432885.1:p.Lys67Gln
ENST00000631044.2:c.*2539A>C ENSP00000486730.1:n.*2539A>C
NM_001126131.1:c.3115A>C NP_001119603.1:p.Lys1039Gln
NM_002693.2:c.3115A>C NP_002684.1:p.Lys1039Gln
NM_001126131.2:c.3115A>C NP_001119603.1:p.Lys1039Gln
NM_002693.3:c.3115A>C MANE Select NP_002684.1:p.Lys1039Gln