Canonical Allele Identifier: CA2194538965
Gene: POLG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.89317393C= , CM000677.2:g.89317393C= GRCh38
NC_000015.9:g.89860624C= , CM000677.1:g.89860624C= GRCh37
NC_000015.8:g.87661628C= NCBI36
NG_008218.1:g.22403G=
NG_011736.1:g.78431C= , LRG_500:g.78431C=
NG_008218.2:g.22403G=

Transcript Alleles

HGVS Amino-acid change
ENST00000636937.2:c.3626G= ENSP00000516154.1:p.Arg1209=
ENST00000268124.11:c.3626G= MANE Select ENSP00000268124.5:p.Arg1209=
ENST00000530292.3:c.3326G= ENSP00000432885.2:n.3326G=
ENST00000635986.2:c.*696G= ENSP00000490653.2:n.*696G=
ENST00000636774.1:c.*2230G= ENSP00000489799.1:n.*2230G=
ENST00000637238.1:c.2534G= ENSP00000490756.1:n.2534G=
ENST00000637264.1:c.2638G=
ENST00000666746.1:c.3203G=
ENST00000672071.1:n.4828G=
ENST00000672695.1:n.1405G=
ENST00000672923.2:n.3626G=
ENST00000268124.9:c.3626G= ENSP00000268124.5:p.Arg1209=
ENST00000442287.6:c.3626G= ENSP00000399851.2:p.Arg1209=
ENST00000526671.1:n.436G=
ENST00000530292.2:c.809G= ENSP00000432885.1:n.809G=
ENST00000631044.2:c.*3050G= ENSP00000486730.1:n.*3050G=
NM_001126131.1:c.3626G= NP_001119603.1:p.Arg1209=
NM_002693.2:c.3626G= NP_002684.1:p.Arg1209=
NM_001126131.2:c.3626G= NP_001119603.1:p.Arg1209=
NM_002693.3:c.3626G= MANE Select NP_002684.1:p.Arg1209=