Canonical Allele Identifier: CA2805167560
Gene: POLG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.89317636_89317637insAGT , CM000677.2:g.89317636_89317637insAGT GRCh38
NC_000015.9:g.89860867_89860868insAGT , CM000677.1:g.89860867_89860868insAGT GRCh37
NC_000015.8:g.87661871_87661872insAGT NCBI36
NG_008218.1:g.22159_22160insACT
NG_011736.1:g.78674_78675insAGT , LRG_500:g.78674_78675insAGT
NG_008218.2:g.22159_22160insACT

Transcript Alleles

HGVS Amino-acid Change
ENST00000636937.2:c.3483-101_3483-100insACT ENSP00000516154.1:n.3483-101_3483-100insACT
ENST00000268124.11:c.3483-101_3483-100insACT MANE Select ENSP00000268124.5:n.3483-101_3483-100insACT
ENST00000530292.3:c.3183-101_3183-100insACT ENSP00000432885.2:n.3183-101_3183-100insACT
ENST00000635986.2:c.*553-101_*553-100insACT ENSP00000490653.2:n.*553-101_*553-100insACT
ENST00000636774.1:c.*2087-101_*2087-100insACT ENSP00000489799.1:n.*2087-101_*2087-100insACT
ENST00000637042.1:n.72-166_72-165insACT
ENST00000637238.1:c.2391-101_2391-100insACT ENSP00000490756.1:n.2391-101_2391-100insACT
ENST00000637264.1:c.2555-161_2555-160insACT
ENST00000666746.1:c.3060-101_3060-100insACT
ENST00000672071.1:n.4584_4585insACT
ENST00000672695.1:n.1262-101_1262-100insACT
ENST00000672923.2:n.3483-101_3483-100insACT
ENST00000268124.9:c.3483-101_3483-100insACT ENSP00000268124.5:n.3483-101_3483-100insACT
ENST00000442287.6:c.3483-101_3483-100insACT ENSP00000399851.2:n.3483-101_3483-100insACT
ENST00000526671.1:n.192_193insACT
ENST00000530292.2:c.666-101_666-100insACT ENSP00000432885.1:n.666-101_666-100insACT
ENST00000631044.2:c.*2907-101_*2907-100insACT ENSP00000486730.1:n.*2907-101_*2907-100insACT
NM_001126131.1:c.3483-101_3483-100insACT NP_001119603.1:n.3483-101_3483-100insACT
NM_002693.2:c.3483-101_3483-100insACT NP_002684.1:n.3483-101_3483-100insACT
NM_001126131.2:c.3483-101_3483-100insACT NP_001119603.1:n.3483-101_3483-100insACT
NM_002693.3:c.3483-101_3483-100insACT MANE Select NP_002684.1:n.3483-101_3483-100insACT