Canonical Allele Identifier: CA2194543298
Gene: POLG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.89319084C= , CM000677.2:g.89319084C= GRCh38
NC_000015.9:g.89862315C= , CM000677.1:g.89862315C= GRCh37
NC_000015.8:g.87663319C= NCBI36
NG_008218.1:g.20712G=
NG_011736.1:g.80122C= , LRG_500:g.80122C=
NG_008218.2:g.20712G=

Transcript Alleles

HGVS Amino-acid change
ENST00000636937.2:c.3120G= ENSP00000516154.1:p.Lys1040=
ENST00000268124.11:c.3120G= MANE Select ENSP00000268124.5:p.Lys1040=
ENST00000530292.3:c.2721G= ENSP00000432885.2:p.Lys907=
ENST00000635986.2:c.*190G= ENSP00000490653.2:n.*190G=
ENST00000636530.1:n.80G=
ENST00000636774.1:c.*1687G= ENSP00000489799.1:n.*1687G=
ENST00000637238.1:c.1929G= ENSP00000490756.1:n.1929G=
ENST00000637264.1:c.2192G=
ENST00000666746.1:c.2697G=
ENST00000672071.1:n.3318G=
ENST00000672695.1:n.297G=
ENST00000672923.2:n.3120G=
ENST00000268124.9:c.3120G= ENSP00000268124.5:p.Lys1040=
ENST00000442287.6:c.3120G= ENSP00000399851.2:p.Lys1040=
ENST00000530292.2:c.204G= ENSP00000432885.1:p.Lys68=
ENST00000631044.2:c.*2544G= ENSP00000486730.1:n.*2544G=
NM_001126131.1:c.3120G= NP_001119603.1:p.Lys1040=
NM_002693.2:c.3120G= NP_002684.1:p.Lys1040=
NM_001126131.2:c.3120G= NP_001119603.1:p.Lys1040=
NM_002693.3:c.3120G= MANE Select NP_002684.1:p.Lys1040=