Canonical Allele Identifier: CA2805167583

Gene: POLG

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.89317671_89317672insACA , CM000677.2:g.89317671_89317672insACA	GRCh38
NC_000015.9:g.89860902_89860903insACA , CM000677.1:g.89860902_89860903insACA	GRCh37
NC_000015.8:g.87661906_87661907insACA	NCBI36
NG_008218.1:g.22124_22125insTGT
NG_011736.1:g.78709_78710insACA , LRG_500:g.78709_78710insACA
NG_008218.2:g.22124_22125insTGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000636937.2:c.3483-136_3483-135insTGT	ENSP00000516154.1:n.3483-136_3483-135insTGT
ENST00000268124.11:c.3483-136_3483-135insTGT MANE Select	ENSP00000268124.5:n.3483-136_3483-135insTGT
ENST00000530292.3:c.3183-136_3183-135insTGT	ENSP00000432885.2:n.3183-136_3183-135insTGT
ENST00000635986.2:c.*553-136_*553-135insTGT	ENSP00000490653.2:n.*553-136_*553-135insTGT
ENST00000636774.1:c.*2087-136_*2087-135insTGT	ENSP00000489799.1:n.*2087-136_*2087-135insTGT
ENST00000637042.1:n.72-201_72-200insTGT
ENST00000637238.1:c.2391-136_2391-135insTGT	ENSP00000490756.1:n.2391-136_2391-135insTGT
ENST00000637264.1:c.2555-196_2555-195insTGT
ENST00000666746.1:c.3060-136_3060-135insTGT
ENST00000672071.1:n.4549_4550insTGT
ENST00000672695.1:n.1262-136_1262-135insTGT
ENST00000672923.2:n.3483-136_3483-135insTGT
ENST00000268124.9:c.3483-136_3483-135insTGT	ENSP00000268124.5:n.3483-136_3483-135insTGT
ENST00000442287.6:c.3483-136_3483-135insTGT	ENSP00000399851.2:n.3483-136_3483-135insTGT
ENST00000526671.1:n.157_158insTGT
ENST00000530292.2:c.666-136_666-135insTGT	ENSP00000432885.1:n.666-136_666-135insTGT
ENST00000631044.2:c.*2907-136_*2907-135insTGT	ENSP00000486730.1:n.*2907-136_*2907-135insTGT
NM_001126131.1:c.3483-136_3483-135insTGT	NP_001119603.1:n.3483-136_3483-135insTGT
NM_002693.2:c.3483-136_3483-135insTGT	NP_002684.1:n.3483-136_3483-135insTGT
NM_001126131.2:c.3483-136_3483-135insTGT	NP_001119603.1:n.3483-136_3483-135insTGT
NM_002693.3:c.3483-136_3483-135insTGT MANE Select	NP_002684.1:n.3483-136_3483-135insTGT