Canonical Allele Identifier: CA2805167595
Gene: POLG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.89317697_89317698insAG , CM000677.2:g.89317697_89317698insAG GRCh38
NC_000015.9:g.89860928_89860929insAG , CM000677.1:g.89860928_89860929insAG GRCh37
NC_000015.8:g.87661932_87661933insAG NCBI36
NG_008218.1:g.22098_22099insCT
NG_011736.1:g.78735_78736insAG , LRG_500:g.78735_78736insAG
NG_008218.2:g.22098_22099insCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000636937.2:c.3483-162_3483-161insCT ENSP00000516154.1:n.3483-162_3483-161insCT
ENST00000268124.11:c.3483-162_3483-161insCT MANE Select ENSP00000268124.5:n.3483-162_3483-161insCT
ENST00000530292.3:c.3183-162_3183-161insCT ENSP00000432885.2:n.3183-162_3183-161insCT
ENST00000635986.2:c.*553-162_*553-161insCT ENSP00000490653.2:n.*553-162_*553-161insCT
ENST00000636774.1:c.*2087-162_*2087-161insCT ENSP00000489799.1:n.*2087-162_*2087-161insCT
ENST00000637042.1:n.72-227_72-226insCT
ENST00000637238.1:c.2391-162_2391-161insCT ENSP00000490756.1:n.2391-162_2391-161insCT
ENST00000637264.1:c.2555-222_2555-221insCT
ENST00000666746.1:c.3060-162_3060-161insCT
ENST00000672071.1:n.4523_4524insCT
ENST00000672695.1:n.1262-162_1262-161insCT
ENST00000672923.2:n.3483-162_3483-161insCT
ENST00000268124.9:c.3483-162_3483-161insCT ENSP00000268124.5:n.3483-162_3483-161insCT
ENST00000442287.6:c.3483-162_3483-161insCT ENSP00000399851.2:n.3483-162_3483-161insCT
ENST00000526671.1:n.131_132insCT
ENST00000530292.2:c.666-162_666-161insCT ENSP00000432885.1:n.666-162_666-161insCT
ENST00000631044.2:c.*2907-162_*2907-161insCT ENSP00000486730.1:n.*2907-162_*2907-161insCT
NM_001126131.1:c.3483-162_3483-161insCT NP_001119603.1:n.3483-162_3483-161insCT
NM_002693.2:c.3483-162_3483-161insCT NP_002684.1:n.3483-162_3483-161insCT
NM_001126131.2:c.3483-162_3483-161insCT NP_001119603.1:n.3483-162_3483-161insCT
NM_002693.3:c.3483-162_3483-161insCT MANE Select NP_002684.1:n.3483-162_3483-161insCT