Canonical Allele Identifier: CA2805168123

Gene: POLG

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.89329146_89329147insACA , CM000677.2:g.89329146_89329147insACA	GRCh38
NC_000015.9:g.89872377_89872378insACA , CM000677.1:g.89872377_89872378insACA	GRCh37
NC_000015.8:g.87673381_87673382insACA	NCBI36
NG_008218.1:g.10649_10650insTGT
NG_008218.2:g.10649_10650insTGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000636937.2:c.856-37_856-36insTGT	ENSP00000516154.1:n.856-37_856-36insTGT
ENST00000268124.11:c.856-37_856-36insTGT MANE Select	ENSP00000268124.5:n.856-37_856-36insTGT
ENST00000530292.3:c.457-37_457-36insTGT	ENSP00000432885.2:n.457-37_457-36insTGT
ENST00000635986.2:c.856-37_856-36insTGT	ENSP00000490653.2:n.856-37_856-36insTGT
ENST00000636774.1:c.856-37_856-36insTGT	ENSP00000489799.1:n.856-37_856-36insTGT
ENST00000666746.1:c.513-37_513-36insTGT
ENST00000672071.1:n.1054-37_1054-36insTGT
ENST00000268124.9:c.856-37_856-36insTGT	ENSP00000268124.5:n.856-37_856-36insTGT
ENST00000442287.6:c.856-37_856-36insTGT	ENSP00000399851.2:n.856-37_856-36insTGT
ENST00000631044.2:c.*239-37_*239-36insTGT	ENSP00000486730.1:n.*239-37_*239-36insTGT
NM_001126131.1:c.856-37_856-36insTGT	NP_001119603.1:n.856-37_856-36insTGT
NM_002693.2:c.856-37_856-36insTGT	NP_002684.1:n.856-37_856-36insTGT
NM_001126131.2:c.856-37_856-36insTGT	NP_001119603.1:n.856-37_856-36insTGT
NM_002693.3:c.856-37_856-36insTGT MANE Select	NP_002684.1:n.856-37_856-36insTGT