Canonical Allele Identifier: CA2805167569
Gene: POLG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.89317642_89317643insAGT , CM000677.2:g.89317642_89317643insAGT GRCh38
NC_000015.9:g.89860873_89860874insAGT , CM000677.1:g.89860873_89860874insAGT GRCh37
NC_000015.8:g.87661877_87661878insAGT NCBI36
NG_008218.1:g.22153_22154insACT
NG_011736.1:g.78680_78681insAGT , LRG_500:g.78680_78681insAGT
NG_008218.2:g.22153_22154insACT

Transcript Alleles

HGVS Amino-acid Change
ENST00000636937.2:c.3483-107_3483-106insACT ENSP00000516154.1:n.3483-107_3483-106insACT
ENST00000268124.11:c.3483-107_3483-106insACT MANE Select ENSP00000268124.5:n.3483-107_3483-106insACT
ENST00000530292.3:c.3183-107_3183-106insACT ENSP00000432885.2:n.3183-107_3183-106insACT
ENST00000635986.2:c.*553-107_*553-106insACT ENSP00000490653.2:n.*553-107_*553-106insACT
ENST00000636774.1:c.*2087-107_*2087-106insACT ENSP00000489799.1:n.*2087-107_*2087-106insACT
ENST00000637042.1:n.72-172_72-171insACT
ENST00000637238.1:c.2391-107_2391-106insACT ENSP00000490756.1:n.2391-107_2391-106insACT
ENST00000637264.1:c.2555-167_2555-166insACT
ENST00000666746.1:c.3060-107_3060-106insACT
ENST00000672071.1:n.4578_4579insACT
ENST00000672695.1:n.1262-107_1262-106insACT
ENST00000672923.2:n.3483-107_3483-106insACT
ENST00000268124.9:c.3483-107_3483-106insACT ENSP00000268124.5:n.3483-107_3483-106insACT
ENST00000442287.6:c.3483-107_3483-106insACT ENSP00000399851.2:n.3483-107_3483-106insACT
ENST00000526671.1:n.186_187insACT
ENST00000530292.2:c.666-107_666-106insACT ENSP00000432885.1:n.666-107_666-106insACT
ENST00000631044.2:c.*2907-107_*2907-106insACT ENSP00000486730.1:n.*2907-107_*2907-106insACT
NM_001126131.1:c.3483-107_3483-106insACT NP_001119603.1:n.3483-107_3483-106insACT
NM_002693.2:c.3483-107_3483-106insACT NP_002684.1:n.3483-107_3483-106insACT
NM_001126131.2:c.3483-107_3483-106insACT NP_001119603.1:n.3483-107_3483-106insACT
NM_002693.3:c.3483-107_3483-106insACT MANE Select NP_002684.1:n.3483-107_3483-106insACT