Canonical Allele Identifier: CA492289085

Gene: POLG

Linked Data

• dbSNP Id: rs1278234644
• MyVariant Identifiers: chr15:g.89864191A>T (hg19) ; chr15:g.89320960A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.89320960A>T , CM000677.2:g.89320960A>T	GRCh38
NC_000015.9:g.89864191A>T , CM000677.1:g.89864191A>T	GRCh37
NC_000015.8:g.87665195A>T	NCBI36
NG_008218.1:g.18836T>A
NG_008218.2:g.18836T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000636937.2:c.2787T>A	ENSP00000516154.1:p.Thr929=
ENST00000268124.11:c.2787T>A MANE Select	ENSP00000268124.5:p.Thr929=
ENST00000530292.3:c.2388T>A	ENSP00000432885.2:p.Thr796=
ENST00000635986.2:c.2787T>A	ENSP00000490653.2:p.Thr929=
ENST00000636774.1:c.*1354T>A	ENSP00000489799.1:n.*1354T>A
ENST00000637238.1:c.1596T>A	ENSP00000490756.1:n.1596T>A
ENST00000637264.1:c.1859T>A
ENST00000666746.1:c.2364T>A
ENST00000670281.1:c.800+1002T>A	ENSP00000499709.1:n.800+1002T>A
ENST00000672071.1:n.2985T>A
ENST00000672923.2:n.2729T>A
ENST00000268124.9:c.2787T>A	ENSP00000268124.5:p.Thr929=
ENST00000442287.6:c.2787T>A	ENSP00000399851.2:p.Thr929=
ENST00000528881.2:c.384T>A
ENST00000530715.5:c.186-91T>A	ENSP00000431395.1:n.186-91T>A
ENST00000631044.2:c.*2211T>A	ENSP00000486730.1:n.*2211T>A
NM_001126131.1:c.2787T>A	NP_001119603.1:p.Thr929=
NM_002693.2:c.2787T>A	NP_002684.1:p.Thr929=
NM_001126131.2:c.2787T>A	NP_001119603.1:p.Thr929=
NM_002693.3:c.2787T>A MANE Select	NP_002684.1:p.Thr929=