Canonical Allele Identifier: CA2805167591
Gene: POLG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.89317685_89317686insA , CM000677.2:g.89317685_89317686insA GRCh38
NC_000015.9:g.89860916_89860917insA , CM000677.1:g.89860916_89860917insA GRCh37
NC_000015.8:g.87661920_87661921insA NCBI36
NG_008218.1:g.22110_22111insT
NG_011736.1:g.78723_78724insA , LRG_500:g.78723_78724insA
NG_008218.2:g.22110_22111insT

Transcript Alleles

HGVS Amino-acid Change
ENST00000636937.2:c.3483-150_3483-149insT ENSP00000516154.1:n.3483-150_3483-149insT
ENST00000268124.11:c.3483-150_3483-149insT MANE Select ENSP00000268124.5:n.3483-150_3483-149insT
ENST00000530292.3:c.3183-150_3183-149insT ENSP00000432885.2:n.3183-150_3183-149insT
ENST00000635986.2:c.*553-150_*553-149insT ENSP00000490653.2:n.*553-150_*553-149insT
ENST00000636774.1:c.*2087-150_*2087-149insT ENSP00000489799.1:n.*2087-150_*2087-149insT
ENST00000637042.1:n.72-215_72-214insT
ENST00000637238.1:c.2391-150_2391-149insT ENSP00000490756.1:n.2391-150_2391-149insT
ENST00000637264.1:c.2555-210_2555-209insT
ENST00000666746.1:c.3060-150_3060-149insT
ENST00000672071.1:n.4535_4536insT
ENST00000672695.1:n.1262-150_1262-149insT
ENST00000672923.2:n.3483-150_3483-149insT
ENST00000268124.9:c.3483-150_3483-149insT ENSP00000268124.5:n.3483-150_3483-149insT
ENST00000442287.6:c.3483-150_3483-149insT ENSP00000399851.2:n.3483-150_3483-149insT
ENST00000526671.1:n.143_144insT
ENST00000530292.2:c.666-150_666-149insT ENSP00000432885.1:n.666-150_666-149insT
ENST00000631044.2:c.*2907-150_*2907-149insT ENSP00000486730.1:n.*2907-150_*2907-149insT
NM_001126131.1:c.3483-150_3483-149insT NP_001119603.1:n.3483-150_3483-149insT
NM_002693.2:c.3483-150_3483-149insT NP_002684.1:n.3483-150_3483-149insT
NM_001126131.2:c.3483-150_3483-149insT NP_001119603.1:n.3483-150_3483-149insT
NM_002693.3:c.3483-150_3483-149insT MANE Select NP_002684.1:n.3483-150_3483-149insT