Canonical Allele Identifier: CA2805167555

Gene: POLG

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.89317630_89317631insAGC , CM000677.2:g.89317630_89317631insAGC	GRCh38
NC_000015.9:g.89860861_89860862insAGC , CM000677.1:g.89860861_89860862insAGC	GRCh37
NC_000015.8:g.87661865_87661866insAGC	NCBI36
NG_008218.1:g.22165_22166insGCT
NG_011736.1:g.78668_78669insAGC , LRG_500:g.78668_78669insAGC
NG_008218.2:g.22165_22166insGCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000636937.2:c.3483-95_3483-94insGCT	ENSP00000516154.1:n.3483-95_3483-94insGCT
ENST00000268124.11:c.3483-95_3483-94insGCT MANE Select	ENSP00000268124.5:n.3483-95_3483-94insGCT
ENST00000530292.3:c.3183-95_3183-94insGCT	ENSP00000432885.2:n.3183-95_3183-94insGCT
ENST00000635986.2:c.*553-95_*553-94insGCT	ENSP00000490653.2:n.*553-95_*553-94insGCT
ENST00000636774.1:c.*2087-95_*2087-94insGCT	ENSP00000489799.1:n.*2087-95_*2087-94insGCT
ENST00000637042.1:n.72-160_72-159insGCT
ENST00000637238.1:c.2391-95_2391-94insGCT	ENSP00000490756.1:n.2391-95_2391-94insGCT
ENST00000637264.1:c.2555-155_2555-154insGCT
ENST00000666746.1:c.3060-95_3060-94insGCT
ENST00000672071.1:n.4590_4591insGCT
ENST00000672695.1:n.1262-95_1262-94insGCT
ENST00000672923.2:n.3483-95_3483-94insGCT
ENST00000268124.9:c.3483-95_3483-94insGCT	ENSP00000268124.5:n.3483-95_3483-94insGCT
ENST00000442287.6:c.3483-95_3483-94insGCT	ENSP00000399851.2:n.3483-95_3483-94insGCT
ENST00000526671.1:n.198_199insGCT
ENST00000530292.2:c.666-95_666-94insGCT	ENSP00000432885.1:n.666-95_666-94insGCT
ENST00000631044.2:c.*2907-95_*2907-94insGCT	ENSP00000486730.1:n.*2907-95_*2907-94insGCT
NM_001126131.1:c.3483-95_3483-94insGCT	NP_001119603.1:n.3483-95_3483-94insGCT
NM_002693.2:c.3483-95_3483-94insGCT	NP_002684.1:n.3483-95_3483-94insGCT
NM_001126131.2:c.3483-95_3483-94insGCT	NP_001119603.1:n.3483-95_3483-94insGCT
NM_002693.3:c.3483-95_3483-94insGCT MANE Select	NP_002684.1:n.3483-95_3483-94insGCT