Canonical Allele Identifier: CA2805167594
Gene: POLG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.89317690_89317691insC , CM000677.2:g.89317690_89317691insC GRCh38
NC_000015.9:g.89860921_89860922insC , CM000677.1:g.89860921_89860922insC GRCh37
NC_000015.8:g.87661925_87661926insC NCBI36
NG_008218.1:g.22105_22106insG
NG_011736.1:g.78728_78729insC , LRG_500:g.78728_78729insC
NG_008218.2:g.22105_22106insG

Transcript Alleles

HGVS Amino-acid Change
ENST00000636937.2:c.3483-155_3483-154insG ENSP00000516154.1:n.3483-155_3483-154insG
ENST00000268124.11:c.3483-155_3483-154insG MANE Select ENSP00000268124.5:n.3483-155_3483-154insG
ENST00000530292.3:c.3183-155_3183-154insG ENSP00000432885.2:n.3183-155_3183-154insG
ENST00000635986.2:c.*553-155_*553-154insG ENSP00000490653.2:n.*553-155_*553-154insG
ENST00000636774.1:c.*2087-155_*2087-154insG ENSP00000489799.1:n.*2087-155_*2087-154insG
ENST00000637042.1:n.72-220_72-219insG
ENST00000637238.1:c.2391-155_2391-154insG ENSP00000490756.1:n.2391-155_2391-154insG
ENST00000637264.1:c.2555-215_2555-214insG
ENST00000666746.1:c.3060-155_3060-154insG
ENST00000672071.1:n.4530_4531insG
ENST00000672695.1:n.1262-155_1262-154insG
ENST00000672923.2:n.3483-155_3483-154insG
ENST00000268124.9:c.3483-155_3483-154insG ENSP00000268124.5:n.3483-155_3483-154insG
ENST00000442287.6:c.3483-155_3483-154insG ENSP00000399851.2:n.3483-155_3483-154insG
ENST00000526671.1:n.138_139insG
ENST00000530292.2:c.666-155_666-154insG ENSP00000432885.1:n.666-155_666-154insG
ENST00000631044.2:c.*2907-155_*2907-154insG ENSP00000486730.1:n.*2907-155_*2907-154insG
NM_001126131.1:c.3483-155_3483-154insG NP_001119603.1:n.3483-155_3483-154insG
NM_002693.2:c.3483-155_3483-154insG NP_002684.1:n.3483-155_3483-154insG
NM_001126131.2:c.3483-155_3483-154insG NP_001119603.1:n.3483-155_3483-154insG
NM_002693.3:c.3483-155_3483-154insG MANE Select NP_002684.1:n.3483-155_3483-154insG