Canonical Allele Identifier: CA2805168178
Gene: POLG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.89329274_89329275insA , CM000677.2:g.89329274_89329275insA GRCh38
NC_000015.9:g.89872505_89872506insA , CM000677.1:g.89872505_89872506insA GRCh37
NC_000015.8:g.87673509_87673510insA NCBI36
NG_008218.1:g.10521_10522insT
NG_008218.2:g.10521_10522insT

Transcript Alleles

HGVS Amino-acid Change
ENST00000636937.2:c.856-165_856-164insT ENSP00000516154.1:n.856-165_856-164insT
ENST00000268124.11:c.856-165_856-164insT MANE Select ENSP00000268124.5:n.856-165_856-164insT
ENST00000530292.3:c.457-165_457-164insT ENSP00000432885.2:n.457-165_457-164insT
ENST00000635986.2:c.856-165_856-164insT ENSP00000490653.2:n.856-165_856-164insT
ENST00000636774.1:c.856-165_856-164insT ENSP00000489799.1:n.856-165_856-164insT
ENST00000666746.1:c.513-165_513-164insT
ENST00000672071.1:n.1054-165_1054-164insT
ENST00000268124.9:c.856-165_856-164insT ENSP00000268124.5:n.856-165_856-164insT
ENST00000442287.6:c.856-165_856-164insT ENSP00000399851.2:n.856-165_856-164insT
ENST00000631044.2:c.*239-165_*239-164insT ENSP00000486730.1:n.*239-165_*239-164insT
NM_001126131.1:c.856-165_856-164insT NP_001119603.1:n.856-165_856-164insT
NM_002693.2:c.856-165_856-164insT NP_002684.1:n.856-165_856-164insT
NM_001126131.2:c.856-165_856-164insT NP_001119603.1:n.856-165_856-164insT
NM_002693.3:c.856-165_856-164insT MANE Select NP_002684.1:n.856-165_856-164insT