Canonical Allele Identifier: CA2630255195
Gene: POLG HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.89317562C>T , CM000677.2:g.89317562C>T GRCh38
NC_000015.9:g.89860793C>T , CM000677.1:g.89860793C>T GRCh37
NC_000015.8:g.87661797C>T NCBI36
NG_008218.1:g.22234G>A
NG_011736.1:g.78600C>T , LRG_500:g.78600C>T
NG_008218.2:g.22234G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000636937.2:c.3483-26G>A ENSP00000516154.1:n.3483-26G>A
ENST00000268124.11:c.3483-26G>A MANE Select ENSP00000268124.5:n.3483-26G>A
ENST00000530292.3:c.3183-26G>A ENSP00000432885.2:n.3183-26G>A
ENST00000635986.2:c.*553-26G>A ENSP00000490653.2:n.*553-26G>A
ENST00000636774.1:c.*2087-26G>A ENSP00000489799.1:n.*2087-26G>A
ENST00000637042.1:n.72-91G>A
ENST00000637238.1:c.2391-26G>A ENSP00000490756.1:n.2391-26G>A
ENST00000637264.1:c.2555-86G>A
ENST00000666746.1:c.3060-26G>A
ENST00000672071.1:n.4659G>A
ENST00000672695.1:n.1262-26G>A
ENST00000672923.2:n.3483-26G>A
ENST00000268124.9:c.3483-26G>A ENSP00000268124.5:n.3483-26G>A
ENST00000442287.6:c.3483-26G>A ENSP00000399851.2:n.3483-26G>A
ENST00000526671.1:n.267G>A
ENST00000530292.2:c.666-26G>A ENSP00000432885.1:n.666-26G>A
ENST00000631044.2:c.*2907-26G>A ENSP00000486730.1:n.*2907-26G>A
NM_001126131.1:c.3483-26G>A NP_001119603.1:n.3483-26G>A
NM_002693.2:c.3483-26G>A NP_002684.1:n.3483-26G>A
NM_001126131.2:c.3483-26G>A NP_001119603.1:n.3483-26G>A
NM_002693.3:c.3483-26G>A MANE Select NP_002684.1:n.3483-26G>A