Canonical Allele Identifier: CA492289416

Gene: POLG

Linked Data

• MyVariant Identifiers: chr15:g.89868827T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.89325596T>C , CM000677.2:g.89325596T>C	GRCh38
NC_000015.9:g.89868827T>C , CM000677.1:g.89868827T>C	GRCh37
NC_000015.8:g.87669831T>C	NCBI36
NG_008218.1:g.14200A>G
NG_008218.2:g.14200A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000636937.2:c.1803A>G	ENSP00000516154.1:p.Lys601=
ENST00000268124.11:c.1803A>G MANE Select	ENSP00000268124.5:p.Lys601=
ENST00000530292.3:c.1404A>G	ENSP00000432885.2:p.Lys468=
ENST00000635986.2:c.1803A>G	ENSP00000490653.2:p.Lys601=
ENST00000636774.1:c.*370A>G	ENSP00000489799.1:n.*370A>G
ENST00000637238.1:c.540A>G	ENSP00000490756.1:p.Lys180=
ENST00000637264.1:c.875A>G
ENST00000666746.1:c.1380A>G
ENST00000670281.1:c.123A>G	ENSP00000499709.1:p.Lys41=
ENST00000672071.1:n.2001A>G
ENST00000672923.2:n.1906A>G
ENST00000268124.9:c.1803A>G	ENSP00000268124.5:p.Lys601=
ENST00000442287.6:c.1803A>G	ENSP00000399851.2:p.Lys601=
ENST00000526314.2:c.185A>G
ENST00000532584.5:n.5A>G
ENST00000631044.2:c.*1186A>G	ENSP00000486730.1:n.*1186A>G
NM_001126131.1:c.1803A>G	NP_001119603.1:p.Lys601=
NM_002693.2:c.1803A>G	NP_002684.1:p.Lys601=
NM_001126131.2:c.1803A>G	NP_001119603.1:p.Lys601=
NM_002693.3:c.1803A>G MANE Select	NP_002684.1:p.Lys601=