Canonical Allele Identifier: CA492080397

Gene: POLG

Linked Data

• ClinVar Variation Id: 3011541
• ClinVar RCV Id: RCV003865164
• MyVariant Identifiers: chr15:g.89873390T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.89330159T>C , CM000677.2:g.89330159T>C	GRCh38
NC_000015.9:g.89873390T>C , CM000677.1:g.89873390T>C	GRCh37
NC_000015.8:g.87674394T>C	NCBI36
NG_008218.1:g.9637A>G
NG_008218.2:g.9637A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000636937.2:c.777A>G	ENSP00000516154.1:p.Arg259=
ENST00000268124.11:c.777A>G MANE Select	ENSP00000268124.5:p.Arg259=
ENST00000530292.3:c.378A>G	ENSP00000432885.2:p.Arg126=
ENST00000635986.2:c.777A>G	ENSP00000490653.2:p.Arg259=
ENST00000636774.1:c.777A>G	ENSP00000489799.1:p.Arg259=
ENST00000666746.1:c.434A>G
ENST00000672071.1:n.975A>G
ENST00000268124.9:c.777A>G	ENSP00000268124.5:p.Arg259=
ENST00000442287.6:c.777A>G	ENSP00000399851.2:p.Arg259=
ENST00000631044.2:c.*160A>G	ENSP00000486730.1:n.*160A>G
NM_001126131.1:c.777A>G	NP_001119603.1:p.Arg259=
NM_002693.2:c.777A>G	NP_002684.1:p.Arg259=
NM_001126131.2:c.777A>G	NP_001119603.1:p.Arg259=
NM_002693.3:c.777A>G MANE Select	NP_002684.1:p.Arg259=