Canonical Allele Identifier: CA492289270

Gene: POLG

Linked Data

• MyVariant Identifiers: chr15:g.89864233G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.89321002G>T , CM000677.2:g.89321002G>T	GRCh38
NC_000015.9:g.89864233G>T , CM000677.1:g.89864233G>T	GRCh37
NC_000015.8:g.87665237G>T	NCBI36
NG_008218.1:g.18794C>A
NG_008218.2:g.18794C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000636937.2:c.2745C>A	ENSP00000516154.1:p.Ala915=
ENST00000268124.11:c.2745C>A MANE Select	ENSP00000268124.5:p.Ala915=
ENST00000530292.3:c.2346C>A	ENSP00000432885.2:p.Ala782=
ENST00000635986.2:c.2745C>A	ENSP00000490653.2:p.Ala915=
ENST00000636774.1:c.*1312C>A	ENSP00000489799.1:n.*1312C>A
ENST00000637238.1:c.1554C>A	ENSP00000490756.1:n.1554C>A
ENST00000637264.1:c.1817C>A
ENST00000666746.1:c.2322C>A
ENST00000670281.1:c.800+960C>A	ENSP00000499709.1:n.800+960C>A
ENST00000672071.1:n.2943C>A
ENST00000672923.2:n.2687C>A
ENST00000268124.9:c.2745C>A	ENSP00000268124.5:p.Ala915=
ENST00000442287.6:c.2745C>A	ENSP00000399851.2:p.Ala915=
ENST00000528881.2:c.342C>A
ENST00000530715.5:c.186-133C>A	ENSP00000431395.1:n.186-133C>A
ENST00000631044.2:c.*2169C>A	ENSP00000486730.1:n.*2169C>A
NM_001126131.1:c.2745C>A	NP_001119603.1:p.Ala915=
NM_002693.2:c.2745C>A	NP_002684.1:p.Ala915=
NM_001126131.2:c.2745C>A	NP_001119603.1:p.Ala915=
NM_002693.3:c.2745C>A MANE Select	NP_002684.1:p.Ala915=