Canonical Allele Identifier: CA2805167537

Gene: POLG

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.89317597_89317598insACAG , CM000677.2:g.89317597_89317598insACAG	GRCh38
NC_000015.9:g.89860828_89860829insACAG , CM000677.1:g.89860828_89860829insACAG	GRCh37
NC_000015.8:g.87661832_87661833insACAG	NCBI36
NG_008218.1:g.22198_22199insCTGT
NG_011736.1:g.78635_78636insACAG , LRG_500:g.78635_78636insACAG
NG_008218.2:g.22198_22199insCTGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000636937.2:c.3483-62_3483-61insCTGT	ENSP00000516154.1:n.3483-62_3483-61insCTGT
ENST00000268124.11:c.3483-62_3483-61insCTGT MANE Select	ENSP00000268124.5:n.3483-62_3483-61insCTGT
ENST00000530292.3:c.3183-62_3183-61insCTGT	ENSP00000432885.2:n.3183-62_3183-61insCTGT
ENST00000635986.2:c.*553-62_*553-61insCTGT	ENSP00000490653.2:n.*553-62_*553-61insCTGT
ENST00000636774.1:c.*2087-62_*2087-61insCTGT	ENSP00000489799.1:n.*2087-62_*2087-61insCTGT
ENST00000637042.1:n.72-127_72-126insCTGT
ENST00000637238.1:c.2391-62_2391-61insCTGT	ENSP00000490756.1:n.2391-62_2391-61insCTGT
ENST00000637264.1:c.2555-122_2555-121insCTGT
ENST00000666746.1:c.3060-62_3060-61insCTGT
ENST00000672071.1:n.4623_4624insCTGT
ENST00000672695.1:n.1262-62_1262-61insCTGT
ENST00000672923.2:n.3483-62_3483-61insCTGT
ENST00000268124.9:c.3483-62_3483-61insCTGT	ENSP00000268124.5:n.3483-62_3483-61insCTGT
ENST00000442287.6:c.3483-62_3483-61insCTGT	ENSP00000399851.2:n.3483-62_3483-61insCTGT
ENST00000526671.1:n.231_232insCTGT
ENST00000530292.2:c.666-62_666-61insCTGT	ENSP00000432885.1:n.666-62_666-61insCTGT
ENST00000631044.2:c.*2907-62_*2907-61insCTGT	ENSP00000486730.1:n.*2907-62_*2907-61insCTGT
NM_001126131.1:c.3483-62_3483-61insCTGT	NP_001119603.1:n.3483-62_3483-61insCTGT
NM_002693.2:c.3483-62_3483-61insCTGT	NP_002684.1:n.3483-62_3483-61insCTGT
NM_001126131.2:c.3483-62_3483-61insCTGT	NP_001119603.1:n.3483-62_3483-61insCTGT
NM_002693.3:c.3483-62_3483-61insCTGT MANE Select	NP_002684.1:n.3483-62_3483-61insCTGT