Canonical Allele Identifier: CA492289528

Gene: POLG

Linked Data

• ClinVar Variation Id: 1653925
• ClinVar RCV Id: RCV002163576
• dbSNP Id: rs2055528821
• MyVariant Identifiers: chr15:g.89870147C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.89326916C>T , CM000677.2:g.89326916C>T	GRCh38
NC_000015.9:g.89870147C>T , CM000677.1:g.89870147C>T	GRCh37
NC_000015.8:g.87671151C>T	NCBI36
NG_008218.1:g.12880G>A
NG_008218.2:g.12880G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000636937.2:c.1581G>A	ENSP00000516154.1:p.Gln527=
ENST00000268124.11:c.1581G>A MANE Select	ENSP00000268124.5:p.Gln527=
ENST00000530292.3:c.1182G>A	ENSP00000432885.2:p.Gln394=
ENST00000635986.2:c.1581G>A	ENSP00000490653.2:p.Gln527=
ENST00000636774.1:c.*148G>A	ENSP00000489799.1:n.*148G>A
ENST00000637238.1:c.318G>A	ENSP00000490756.1:p.Gln106=
ENST00000637264.1:c.653G>A
ENST00000666746.1:c.1158G>A
ENST00000672071.1:n.1779G>A
ENST00000672923.2:n.1684G>A
ENST00000268124.9:c.1581G>A	ENSP00000268124.5:p.Gln527=
ENST00000442287.6:c.1581G>A	ENSP00000399851.2:p.Gln527=
ENST00000631044.2:c.*964G>A	ENSP00000486730.1:n.*964G>A
NM_001126131.1:c.1581G>A	NP_001119603.1:p.Gln527=
NM_002693.2:c.1581G>A	NP_002684.1:p.Gln527=
NM_001126131.2:c.1581G>A	NP_001119603.1:p.Gln527=
NM_002693.3:c.1581G>A MANE Select	NP_002684.1:p.Gln527=