Canonical Allele Identifier: CA492289246

Gene: POLG

Linked Data

• MyVariant Identifiers: chr15:g.89868749C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.89325518C>A , CM000677.2:g.89325518C>A	GRCh38
NC_000015.9:g.89868749C>A , CM000677.1:g.89868749C>A	GRCh37
NC_000015.8:g.87669753C>A	NCBI36
NG_008218.1:g.14278G>T
NG_008218.2:g.14278G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000636937.2:c.1881G>T	ENSP00000516154.1:p.Arg627=
ENST00000268124.11:c.1881G>T MANE Select	ENSP00000268124.5:p.Arg627=
ENST00000530292.3:c.1482G>T	ENSP00000432885.2:p.Arg494=
ENST00000635986.2:c.1881G>T	ENSP00000490653.2:p.Arg627=
ENST00000636774.1:c.*448G>T	ENSP00000489799.1:n.*448G>T
ENST00000637238.1:c.618G>T	ENSP00000490756.1:p.Arg206=
ENST00000637264.1:c.953G>T
ENST00000666746.1:c.1458G>T
ENST00000670281.1:c.201G>T	ENSP00000499709.1:p.Arg67=
ENST00000672071.1:n.2079G>T
ENST00000672923.2:n.1984G>T
ENST00000268124.9:c.1881G>T	ENSP00000268124.5:p.Arg627=
ENST00000442287.6:c.1881G>T	ENSP00000399851.2:p.Arg627=
ENST00000526314.2:c.263G>T
ENST00000526398.1:c.70G>T
ENST00000532584.5:n.83G>T
ENST00000631044.2:c.*1264G>T	ENSP00000486730.1:n.*1264G>T
NM_001126131.1:c.1881G>T	NP_001119603.1:p.Arg627=
NM_002693.2:c.1881G>T	NP_002684.1:p.Arg627=
NM_001126131.2:c.1881G>T	NP_001119603.1:p.Arg627=
NM_002693.3:c.1881G>T MANE Select	NP_002684.1:p.Arg627=