Canonical Allele Identifier: CA492289798

Gene: POLG

Linked Data

• MyVariant Identifiers: chr15:g.89871976C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.89328745C>T , CM000677.2:g.89328745C>T	GRCh38
NC_000015.9:g.89871976C>T , CM000677.1:g.89871976C>T	GRCh37
NC_000015.8:g.87672980C>T	NCBI36
NG_008218.1:g.11051G>A
NG_008218.2:g.11051G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000636937.2:c.1110G>A	ENSP00000516154.1:p.Glu370=
ENST00000268124.11:c.1110G>A MANE Select	ENSP00000268124.5:p.Glu370=
ENST00000530292.3:c.711G>A	ENSP00000432885.2:p.Glu237=
ENST00000635986.2:c.1110G>A	ENSP00000490653.2:p.Glu370=
ENST00000636774.1:c.1110G>A	ENSP00000489799.1:p.Glu370=
ENST00000637264.1:c.182G>A
ENST00000666746.1:c.767G>A
ENST00000672071.1:n.1308G>A
ENST00000672923.2:n.107G>A
ENST00000268124.9:c.1110G>A	ENSP00000268124.5:p.Glu370=
ENST00000442287.6:c.1110G>A	ENSP00000399851.2:p.Glu370=
ENST00000631044.2:c.*493G>A	ENSP00000486730.1:n.*493G>A
NM_001126131.1:c.1110G>A	NP_001119603.1:p.Glu370=
NM_002693.2:c.1110G>A	NP_002684.1:p.Glu370=
NM_001126131.2:c.1110G>A	NP_001119603.1:p.Glu370=
NM_002693.3:c.1110G>A MANE Select	NP_002684.1:p.Glu370=