Canonical Allele Identifier: CA2805167561

Gene: POLG

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.89317637_89317638insACAG , CM000677.2:g.89317637_89317638insACAG	GRCh38
NC_000015.9:g.89860868_89860869insACAG , CM000677.1:g.89860868_89860869insACAG	GRCh37
NC_000015.8:g.87661872_87661873insACAG	NCBI36
NG_008218.1:g.22158_22159insCTGT
NG_011736.1:g.78675_78676insACAG , LRG_500:g.78675_78676insACAG
NG_008218.2:g.22158_22159insCTGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000636937.2:c.3483-102_3483-101insCTGT	ENSP00000516154.1:n.3483-102_3483-101insCTGT
ENST00000268124.11:c.3483-102_3483-101insCTGT MANE Select	ENSP00000268124.5:n.3483-102_3483-101insCTGT
ENST00000530292.3:c.3183-102_3183-101insCTGT	ENSP00000432885.2:n.3183-102_3183-101insCTGT
ENST00000635986.2:c.*553-102_*553-101insCTGT	ENSP00000490653.2:n.*553-102_*553-101insCTGT
ENST00000636774.1:c.*2087-102_*2087-101insCTGT	ENSP00000489799.1:n.*2087-102_*2087-101insCTGT
ENST00000637042.1:n.72-167_72-166insCTGT
ENST00000637238.1:c.2391-102_2391-101insCTGT	ENSP00000490756.1:n.2391-102_2391-101insCTGT
ENST00000637264.1:c.2555-162_2555-161insCTGT
ENST00000666746.1:c.3060-102_3060-101insCTGT
ENST00000672071.1:n.4583_4584insCTGT
ENST00000672695.1:n.1262-102_1262-101insCTGT
ENST00000672923.2:n.3483-102_3483-101insCTGT
ENST00000268124.9:c.3483-102_3483-101insCTGT	ENSP00000268124.5:n.3483-102_3483-101insCTGT
ENST00000442287.6:c.3483-102_3483-101insCTGT	ENSP00000399851.2:n.3483-102_3483-101insCTGT
ENST00000526671.1:n.191_192insCTGT
ENST00000530292.2:c.666-102_666-101insCTGT	ENSP00000432885.1:n.666-102_666-101insCTGT
ENST00000631044.2:c.*2907-102_*2907-101insCTGT	ENSP00000486730.1:n.*2907-102_*2907-101insCTGT
NM_001126131.1:c.3483-102_3483-101insCTGT	NP_001119603.1:n.3483-102_3483-101insCTGT
NM_002693.2:c.3483-102_3483-101insCTGT	NP_002684.1:n.3483-102_3483-101insCTGT
NM_001126131.2:c.3483-102_3483-101insCTGT	NP_001119603.1:n.3483-102_3483-101insCTGT
NM_002693.3:c.3483-102_3483-101insCTGT MANE Select	NP_002684.1:n.3483-102_3483-101insCTGT