Canonical Allele Identifier: CA492080595

Gene: POLG

Linked Data

• MyVariant Identifiers: chr15:g.89873426C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.89330195C>G , CM000677.2:g.89330195C>G	GRCh38
NC_000015.9:g.89873426C>G , CM000677.1:g.89873426C>G	GRCh37
NC_000015.8:g.87674430C>G	NCBI36
NG_008218.1:g.9601G>C
NG_008218.2:g.9601G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000636937.2:c.741G>C	ENSP00000516154.1:p.Leu247=
ENST00000268124.11:c.741G>C MANE Select	ENSP00000268124.5:p.Leu247=
ENST00000530292.3:c.342G>C	ENSP00000432885.2:p.Leu114=
ENST00000635986.2:c.741G>C	ENSP00000490653.2:p.Leu247=
ENST00000636774.1:c.741G>C	ENSP00000489799.1:p.Leu247=
ENST00000666746.1:c.398G>C
ENST00000672071.1:n.939G>C
ENST00000268124.9:c.741G>C	ENSP00000268124.5:p.Leu247=
ENST00000442287.6:c.741G>C	ENSP00000399851.2:p.Leu247=
ENST00000631044.2:c.*124G>C	ENSP00000486730.1:n.*124G>C
NM_001126131.1:c.741G>C	NP_001119603.1:p.Leu247=
NM_002693.2:c.741G>C	NP_002684.1:p.Leu247=
NM_001126131.2:c.741G>C	NP_001119603.1:p.Leu247=
NM_002693.3:c.741G>C MANE Select	NP_002684.1:p.Leu247=