Canonical Allele Identifier: CA492289261

Gene: POLG

Linked Data

• MyVariant Identifiers: chr15:g.89868755A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.89325524A>G , CM000677.2:g.89325524A>G	GRCh38
NC_000015.9:g.89868755A>G , CM000677.1:g.89868755A>G	GRCh37
NC_000015.8:g.87669759A>G	NCBI36
NG_008218.1:g.14272T>C
NG_008218.2:g.14272T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000636937.2:c.1875T>C	ENSP00000516154.1:p.Pro625=
ENST00000268124.11:c.1875T>C MANE Select	ENSP00000268124.5:p.Pro625=
ENST00000530292.3:c.1476T>C	ENSP00000432885.2:p.Pro492=
ENST00000635986.2:c.1875T>C	ENSP00000490653.2:p.Pro625=
ENST00000636774.1:c.*442T>C	ENSP00000489799.1:n.*442T>C
ENST00000637238.1:c.612T>C	ENSP00000490756.1:p.Pro204=
ENST00000637264.1:c.947T>C
ENST00000666746.1:c.1452T>C
ENST00000670281.1:c.195T>C	ENSP00000499709.1:p.Pro65=
ENST00000672071.1:n.2073T>C
ENST00000672923.2:n.1978T>C
ENST00000268124.9:c.1875T>C	ENSP00000268124.5:p.Pro625=
ENST00000442287.6:c.1875T>C	ENSP00000399851.2:p.Pro625=
ENST00000526314.2:c.257T>C
ENST00000526398.1:c.64T>C
ENST00000532584.5:n.77T>C
ENST00000631044.2:c.*1258T>C	ENSP00000486730.1:n.*1258T>C
NM_001126131.1:c.1875T>C	NP_001119603.1:p.Pro625=
NM_002693.2:c.1875T>C	NP_002684.1:p.Pro625=
NM_001126131.2:c.1875T>C	NP_001119603.1:p.Pro625=
NM_002693.3:c.1875T>C MANE Select	NP_002684.1:p.Pro625=