Canonical Allele Identifier: CA492289186

Gene: POLG

Linked Data

• MyVariant Identifiers: chr15:g.89868704T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.89325473T>C , CM000677.2:g.89325473T>C	GRCh38
NC_000015.9:g.89868704T>C , CM000677.1:g.89868704T>C	GRCh37
NC_000015.8:g.87669708T>C	NCBI36
NG_008218.1:g.14323A>G
NG_008218.2:g.14323A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000636937.2:c.1926A>G	ENSP00000516154.1:p.Ser642=
ENST00000268124.11:c.1926A>G MANE Select	ENSP00000268124.5:p.Ser642=
ENST00000530292.3:c.1527A>G	ENSP00000432885.2:p.Ser509=
ENST00000635986.2:c.1926A>G	ENSP00000490653.2:p.Ser642=
ENST00000636774.1:c.*493A>G	ENSP00000489799.1:n.*493A>G
ENST00000637238.1:c.646+17A>G	ENSP00000490756.1:n.646+17A>G
ENST00000637264.1:c.998A>G
ENST00000666746.1:c.1503A>G
ENST00000670281.1:c.246A>G	ENSP00000499709.1:p.Ser82=
ENST00000672071.1:n.2124A>G
ENST00000672923.2:n.2029A>G
ENST00000268124.9:c.1926A>G	ENSP00000268124.5:p.Ser642=
ENST00000442287.6:c.1926A>G	ENSP00000399851.2:p.Ser642=
ENST00000526314.2:c.308A>G
ENST00000526398.1:c.115A>G
ENST00000526573.1:n.12A>G
ENST00000532584.5:n.128A>G
ENST00000631044.2:c.*1309A>G	ENSP00000486730.1:n.*1309A>G
NM_001126131.1:c.1926A>G	NP_001119603.1:p.Ser642=
NM_002693.2:c.1926A>G	NP_002684.1:p.Ser642=
NM_001126131.2:c.1926A>G	NP_001119603.1:p.Ser642=
NM_002693.3:c.1926A>G MANE Select	NP_002684.1:p.Ser642=