Canonical Allele Identifier: CA492289485

Gene: POLG

Linked Data

• MyVariant Identifiers: chr15:g.89868857G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.89325626G>C , CM000677.2:g.89325626G>C	GRCh38
NC_000015.9:g.89868857G>C , CM000677.1:g.89868857G>C	GRCh37
NC_000015.8:g.87669861G>C	NCBI36
NG_008218.1:g.14170C>G
NG_008218.2:g.14170C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000636937.2:c.1773C>G	ENSP00000516154.1:p.Leu591=
ENST00000268124.11:c.1773C>G MANE Select	ENSP00000268124.5:p.Leu591=
ENST00000530292.3:c.1374C>G	ENSP00000432885.2:p.Leu458=
ENST00000635986.2:c.1773C>G	ENSP00000490653.2:p.Leu591=
ENST00000636774.1:c.*340C>G	ENSP00000489799.1:n.*340C>G
ENST00000637238.1:c.510C>G	ENSP00000490756.1:p.Leu170=
ENST00000637264.1:c.845C>G
ENST00000666746.1:c.1350C>G
ENST00000670281.1:c.93C>G	ENSP00000499709.1:p.Leu31=
ENST00000672071.1:n.1971C>G
ENST00000672923.2:n.1876C>G
ENST00000268124.9:c.1773C>G	ENSP00000268124.5:p.Leu591=
ENST00000442287.6:c.1773C>G	ENSP00000399851.2:p.Leu591=
ENST00000526314.2:c.155C>G
ENST00000631044.2:c.*1156C>G	ENSP00000486730.1:n.*1156C>G
NM_001126131.1:c.1773C>G	NP_001119603.1:p.Leu591=
NM_002693.2:c.1773C>G	NP_002684.1:p.Leu591=
NM_001126131.2:c.1773C>G	NP_001119603.1:p.Leu591=
NM_002693.3:c.1773C>G MANE Select	NP_002684.1:p.Leu591=