Canonical Allele Identifier: CA2805168130

Gene: POLG

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.89329165_89329166insA , CM000677.2:g.89329165_89329166insA	GRCh38
NC_000015.9:g.89872396_89872397insA , CM000677.1:g.89872396_89872397insA	GRCh37
NC_000015.8:g.87673400_87673401insA	NCBI36
NG_008218.1:g.10630_10631insT
NG_008218.2:g.10630_10631insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000636937.2:c.856-56_856-55insT	ENSP00000516154.1:n.856-56_856-55insT
ENST00000268124.11:c.856-56_856-55insT MANE Select	ENSP00000268124.5:n.856-56_856-55insT
ENST00000530292.3:c.457-56_457-55insT	ENSP00000432885.2:n.457-56_457-55insT
ENST00000635986.2:c.856-56_856-55insT	ENSP00000490653.2:n.856-56_856-55insT
ENST00000636774.1:c.856-56_856-55insT	ENSP00000489799.1:n.856-56_856-55insT
ENST00000666746.1:c.513-56_513-55insT
ENST00000672071.1:n.1054-56_1054-55insT
ENST00000268124.9:c.856-56_856-55insT	ENSP00000268124.5:n.856-56_856-55insT
ENST00000442287.6:c.856-56_856-55insT	ENSP00000399851.2:n.856-56_856-55insT
ENST00000631044.2:c.*239-56_*239-55insT	ENSP00000486730.1:n.*239-56_*239-55insT
NM_001126131.1:c.856-56_856-55insT	NP_001119603.1:n.856-56_856-55insT
NM_002693.2:c.856-56_856-55insT	NP_002684.1:n.856-56_856-55insT
NM_001126131.2:c.856-56_856-55insT	NP_001119603.1:n.856-56_856-55insT
NM_002693.3:c.856-56_856-55insT MANE Select	NP_002684.1:n.856-56_856-55insT