Canonical Allele Identifier: CA2805167536
Gene: POLG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.89317597_89317598insAC , CM000677.2:g.89317597_89317598insAC GRCh38
NC_000015.9:g.89860828_89860829insAC , CM000677.1:g.89860828_89860829insAC GRCh37
NC_000015.8:g.87661832_87661833insAC NCBI36
NG_008218.1:g.22199_22200insTG
NG_011736.1:g.78635_78636insAC , LRG_500:g.78635_78636insAC
NG_008218.2:g.22199_22200insTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000636937.2:c.3483-61_3483-60insTG ENSP00000516154.1:n.3483-61_3483-60insTG
ENST00000268124.11:c.3483-61_3483-60insTG MANE Select ENSP00000268124.5:n.3483-61_3483-60insTG
ENST00000530292.3:c.3183-61_3183-60insTG ENSP00000432885.2:n.3183-61_3183-60insTG
ENST00000635986.2:c.*553-61_*553-60insTG ENSP00000490653.2:n.*553-61_*553-60insTG
ENST00000636774.1:c.*2087-61_*2087-60insTG ENSP00000489799.1:n.*2087-61_*2087-60insTG
ENST00000637042.1:n.72-126_72-125insTG
ENST00000637238.1:c.2391-61_2391-60insTG ENSP00000490756.1:n.2391-61_2391-60insTG
ENST00000637264.1:c.2555-121_2555-120insTG
ENST00000666746.1:c.3060-61_3060-60insTG
ENST00000672071.1:n.4624_4625insTG
ENST00000672695.1:n.1262-61_1262-60insTG
ENST00000672923.2:n.3483-61_3483-60insTG
ENST00000268124.9:c.3483-61_3483-60insTG ENSP00000268124.5:n.3483-61_3483-60insTG
ENST00000442287.6:c.3483-61_3483-60insTG ENSP00000399851.2:n.3483-61_3483-60insTG
ENST00000526671.1:n.232_233insTG
ENST00000530292.2:c.666-61_666-60insTG ENSP00000432885.1:n.666-61_666-60insTG
ENST00000631044.2:c.*2907-61_*2907-60insTG ENSP00000486730.1:n.*2907-61_*2907-60insTG
NM_001126131.1:c.3483-61_3483-60insTG NP_001119603.1:n.3483-61_3483-60insTG
NM_002693.2:c.3483-61_3483-60insTG NP_002684.1:n.3483-61_3483-60insTG
NM_001126131.2:c.3483-61_3483-60insTG NP_001119603.1:n.3483-61_3483-60insTG
NM_002693.3:c.3483-61_3483-60insTG MANE Select NP_002684.1:n.3483-61_3483-60insTG