Canonical Allele Identifier: CA2805167579

Gene: POLG

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.89317668_89317669insGAG , CM000677.2:g.89317668_89317669insGAG	GRCh38
NC_000015.9:g.89860899_89860900insGAG , CM000677.1:g.89860899_89860900insGAG	GRCh37
NC_000015.8:g.87661903_87661904insGAG	NCBI36
NG_008218.1:g.22127_22128insCTC
NG_011736.1:g.78706_78707insGAG , LRG_500:g.78706_78707insGAG
NG_008218.2:g.22127_22128insCTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000636937.2:c.3483-133_3483-132insCTC	ENSP00000516154.1:n.3483-133_3483-132insCTC
ENST00000268124.11:c.3483-133_3483-132insCTC MANE Select	ENSP00000268124.5:n.3483-133_3483-132insCTC
ENST00000530292.3:c.3183-133_3183-132insCTC	ENSP00000432885.2:n.3183-133_3183-132insCTC
ENST00000635986.2:c.*553-133_*553-132insCTC	ENSP00000490653.2:n.*553-133_*553-132insCTC
ENST00000636774.1:c.*2087-133_*2087-132insCTC	ENSP00000489799.1:n.*2087-133_*2087-132insCTC
ENST00000637042.1:n.72-198_72-197insCTC
ENST00000637238.1:c.2391-133_2391-132insCTC	ENSP00000490756.1:n.2391-133_2391-132insCTC
ENST00000637264.1:c.2555-193_2555-192insCTC
ENST00000666746.1:c.3060-133_3060-132insCTC
ENST00000672071.1:n.4552_4553insCTC
ENST00000672695.1:n.1262-133_1262-132insCTC
ENST00000672923.2:n.3483-133_3483-132insCTC
ENST00000268124.9:c.3483-133_3483-132insCTC	ENSP00000268124.5:n.3483-133_3483-132insCTC
ENST00000442287.6:c.3483-133_3483-132insCTC	ENSP00000399851.2:n.3483-133_3483-132insCTC
ENST00000526671.1:n.160_161insCTC
ENST00000530292.2:c.666-133_666-132insCTC	ENSP00000432885.1:n.666-133_666-132insCTC
ENST00000631044.2:c.*2907-133_*2907-132insCTC	ENSP00000486730.1:n.*2907-133_*2907-132insCTC
NM_001126131.1:c.3483-133_3483-132insCTC	NP_001119603.1:n.3483-133_3483-132insCTC
NM_002693.2:c.3483-133_3483-132insCTC	NP_002684.1:n.3483-133_3483-132insCTC
NM_001126131.2:c.3483-133_3483-132insCTC	NP_001119603.1:n.3483-133_3483-132insCTC
NM_002693.3:c.3483-133_3483-132insCTC MANE Select	NP_002684.1:n.3483-133_3483-132insCTC