Canonical Allele Identifier: CA2805167585
Gene: POLG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.89317680_89317681insACA , CM000677.2:g.89317680_89317681insACA GRCh38
NC_000015.9:g.89860911_89860912insACA , CM000677.1:g.89860911_89860912insACA GRCh37
NC_000015.8:g.87661915_87661916insACA NCBI36
NG_008218.1:g.22115_22116insTGT
NG_011736.1:g.78718_78719insACA , LRG_500:g.78718_78719insACA
NG_008218.2:g.22115_22116insTGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000636937.2:c.3483-145_3483-144insTGT ENSP00000516154.1:n.3483-145_3483-144insTGT
ENST00000268124.11:c.3483-145_3483-144insTGT MANE Select ENSP00000268124.5:n.3483-145_3483-144insTGT
ENST00000530292.3:c.3183-145_3183-144insTGT ENSP00000432885.2:n.3183-145_3183-144insTGT
ENST00000635986.2:c.*553-145_*553-144insTGT ENSP00000490653.2:n.*553-145_*553-144insTGT
ENST00000636774.1:c.*2087-145_*2087-144insTGT ENSP00000489799.1:n.*2087-145_*2087-144insTGT
ENST00000637042.1:n.72-210_72-209insTGT
ENST00000637238.1:c.2391-145_2391-144insTGT ENSP00000490756.1:n.2391-145_2391-144insTGT
ENST00000637264.1:c.2555-205_2555-204insTGT
ENST00000666746.1:c.3060-145_3060-144insTGT
ENST00000672071.1:n.4540_4541insTGT
ENST00000672695.1:n.1262-145_1262-144insTGT
ENST00000672923.2:n.3483-145_3483-144insTGT
ENST00000268124.9:c.3483-145_3483-144insTGT ENSP00000268124.5:n.3483-145_3483-144insTGT
ENST00000442287.6:c.3483-145_3483-144insTGT ENSP00000399851.2:n.3483-145_3483-144insTGT
ENST00000526671.1:n.148_149insTGT
ENST00000530292.2:c.666-145_666-144insTGT ENSP00000432885.1:n.666-145_666-144insTGT
ENST00000631044.2:c.*2907-145_*2907-144insTGT ENSP00000486730.1:n.*2907-145_*2907-144insTGT
NM_001126131.1:c.3483-145_3483-144insTGT NP_001119603.1:n.3483-145_3483-144insTGT
NM_002693.2:c.3483-145_3483-144insTGT NP_002684.1:n.3483-145_3483-144insTGT
NM_001126131.2:c.3483-145_3483-144insTGT NP_001119603.1:n.3483-145_3483-144insTGT
NM_002693.3:c.3483-145_3483-144insTGT MANE Select NP_002684.1:n.3483-145_3483-144insTGT