Canonical Allele Identifier: CA2630254862
Gene: POLG HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.89317304T>A , CM000677.2:g.89317304T>A GRCh38
NC_000015.9:g.89860535T>A , CM000677.1:g.89860535T>A GRCh37
NC_000015.8:g.87661539T>A NCBI36
NG_008218.1:g.22492A>T
NG_011736.1:g.78342T>A , LRG_500:g.78342T>A
NG_008218.2:g.22492A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000636937.2:c.3643+72A>T ENSP00000516154.1:n.3643+72A>T
ENST00000268124.11:c.3643+72A>T MANE Select ENSP00000268124.5:n.3643+72A>T
ENST00000530292.3:c.3343+72A>T ENSP00000432885.2:n.3343+72A>T
ENST00000635986.2:c.*713+72A>T ENSP00000490653.2:n.*713+72A>T
ENST00000636774.1:c.*2247+72A>T ENSP00000489799.1:n.*2247+72A>T
ENST00000637238.1:c.2551+72A>T ENSP00000490756.1:n.2551+72A>T
ENST00000637264.1:c.2655+72A>T
ENST00000666746.1:c.3220+72A>T
ENST00000672071.1:n.4845+72A>T
ENST00000672695.1:n.1422+72A>T
ENST00000672923.2:n.3643+72A>T
ENST00000268124.9:c.3643+72A>T ENSP00000268124.5:n.3643+72A>T
ENST00000442287.6:c.3643+72A>T ENSP00000399851.2:n.3643+72A>T
ENST00000526671.1:n.453+72A>T
ENST00000530292.2:c.826+72A>T ENSP00000432885.1:n.826+72A>T
ENST00000631044.2:c.*3067+72A>T ENSP00000486730.1:n.*3067+72A>T
NM_001126131.1:c.3643+72A>T NP_001119603.1:n.3643+72A>T
NM_002693.2:c.3643+72A>T NP_002684.1:n.3643+72A>T
NM_001126131.2:c.3643+72A>T NP_001119603.1:n.3643+72A>T
NM_002693.3:c.3643+72A>T MANE Select NP_002684.1:n.3643+72A>T