Canonical Allele Identifier: CA492076170

Gene: POLG

Linked Data

• MyVariant Identifiers: chr15:g.89866635C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.89323404C>T , CM000677.2:g.89323404C>T	GRCh38
NC_000015.9:g.89866635C>T , CM000677.1:g.89866635C>T	GRCh37
NC_000015.8:g.87667639C>T	NCBI36
NG_008218.1:g.16392G>A
NG_008218.2:g.16392G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000636937.2:c.2265G>A	ENSP00000516154.1:p.Lys755=
ENST00000268124.11:c.2265G>A MANE Select	ENSP00000268124.5:p.Lys755=
ENST00000530292.3:c.1866G>A	ENSP00000432885.2:p.Lys622=
ENST00000635986.2:c.2265G>A	ENSP00000490653.2:p.Lys755=
ENST00000636774.1:c.*832G>A	ENSP00000489799.1:n.*832G>A
ENST00000637238.1:c.962G>A	ENSP00000490756.1:n.962G>A
ENST00000637264.1:c.1337G>A
ENST00000666746.1:c.1842G>A
ENST00000670281.1:c.585G>A	ENSP00000499709.1:p.Lys195=
ENST00000672071.1:n.2463G>A
ENST00000672923.2:n.2368G>A
ENST00000268124.9:c.2265G>A	ENSP00000268124.5:p.Lys755=
ENST00000442287.6:c.2265G>A	ENSP00000399851.2:p.Lys755=
ENST00000526314.2:c.539+411G>A
ENST00000526398.1:c.414G>A
ENST00000528881.2:c.34G>A
ENST00000530715.5:c.24G>A	ENSP00000431395.1:p.Lys8=
ENST00000532584.5:n.467G>A
ENST00000631044.2:c.*1689G>A	ENSP00000486730.1:n.*1689G>A
NM_001126131.1:c.2265G>A	NP_001119603.1:p.Lys755=
NM_002693.2:c.2265G>A	NP_002684.1:p.Lys755=
NM_001126131.2:c.2265G>A	NP_001119603.1:p.Lys755=
NM_002693.3:c.2265G>A MANE Select	NP_002684.1:p.Lys755=