Canonical Allele Identifier: CA2805167550
Gene: POLG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.89317620_89317621insAC , CM000677.2:g.89317620_89317621insAC GRCh38
NC_000015.9:g.89860851_89860852insAC , CM000677.1:g.89860851_89860852insAC GRCh37
NC_000015.8:g.87661855_87661856insAC NCBI36
NG_008218.1:g.22175_22176insGT
NG_011736.1:g.78658_78659insAC , LRG_500:g.78658_78659insAC
NG_008218.2:g.22175_22176insGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000636937.2:c.3483-85_3483-84insGT ENSP00000516154.1:n.3483-85_3483-84insGT
ENST00000268124.11:c.3483-85_3483-84insGT MANE Select ENSP00000268124.5:n.3483-85_3483-84insGT
ENST00000530292.3:c.3183-85_3183-84insGT ENSP00000432885.2:n.3183-85_3183-84insGT
ENST00000635986.2:c.*553-85_*553-84insGT ENSP00000490653.2:n.*553-85_*553-84insGT
ENST00000636774.1:c.*2087-85_*2087-84insGT ENSP00000489799.1:n.*2087-85_*2087-84insGT
ENST00000637042.1:n.72-150_72-149insGT
ENST00000637238.1:c.2391-85_2391-84insGT ENSP00000490756.1:n.2391-85_2391-84insGT
ENST00000637264.1:c.2555-145_2555-144insGT
ENST00000666746.1:c.3060-85_3060-84insGT
ENST00000672071.1:n.4600_4601insGT
ENST00000672695.1:n.1262-85_1262-84insGT
ENST00000672923.2:n.3483-85_3483-84insGT
ENST00000268124.9:c.3483-85_3483-84insGT ENSP00000268124.5:n.3483-85_3483-84insGT
ENST00000442287.6:c.3483-85_3483-84insGT ENSP00000399851.2:n.3483-85_3483-84insGT
ENST00000526671.1:n.208_209insGT
ENST00000530292.2:c.666-85_666-84insGT ENSP00000432885.1:n.666-85_666-84insGT
ENST00000631044.2:c.*2907-85_*2907-84insGT ENSP00000486730.1:n.*2907-85_*2907-84insGT
NM_001126131.1:c.3483-85_3483-84insGT NP_001119603.1:n.3483-85_3483-84insGT
NM_002693.2:c.3483-85_3483-84insGT NP_002684.1:n.3483-85_3483-84insGT
NM_001126131.2:c.3483-85_3483-84insGT NP_001119603.1:n.3483-85_3483-84insGT
NM_002693.3:c.3483-85_3483-84insGT MANE Select NP_002684.1:n.3483-85_3483-84insGT