Canonical Allele Identifier: CA492289280

Gene: POLG

Linked Data

• gnomAD v4: 15-89325542-G-C
• MyVariant Identifiers: chr15:g.89868773G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.89325542G>C , CM000677.2:g.89325542G>C	GRCh38
NC_000015.9:g.89868773G>C , CM000677.1:g.89868773G>C	GRCh37
NC_000015.8:g.87669777G>C	NCBI36
NG_008218.1:g.14254C>G
NG_008218.2:g.14254C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000636937.2:c.1857C>G	ENSP00000516154.1:p.Gly619=
ENST00000268124.11:c.1857C>G MANE Select	ENSP00000268124.5:p.Gly619=
ENST00000530292.3:c.1458C>G	ENSP00000432885.2:p.Gly486=
ENST00000635986.2:c.1857C>G	ENSP00000490653.2:p.Gly619=
ENST00000636774.1:c.*424C>G	ENSP00000489799.1:n.*424C>G
ENST00000637238.1:c.594C>G	ENSP00000490756.1:p.Gly198=
ENST00000637264.1:c.929C>G
ENST00000666746.1:c.1434C>G
ENST00000670281.1:c.177C>G	ENSP00000499709.1:p.Gly59=
ENST00000672071.1:n.2055C>G
ENST00000672923.2:n.1960C>G
ENST00000268124.9:c.1857C>G	ENSP00000268124.5:p.Gly619=
ENST00000442287.6:c.1857C>G	ENSP00000399851.2:p.Gly619=
ENST00000526314.2:c.239C>G
ENST00000526398.1:c.46C>G
ENST00000532584.5:n.59C>G
ENST00000631044.2:c.*1240C>G	ENSP00000486730.1:n.*1240C>G
NM_001126131.1:c.1857C>G	NP_001119603.1:p.Gly619=
NM_002693.2:c.1857C>G	NP_002684.1:p.Gly619=
NM_001126131.2:c.1857C>G	NP_001119603.1:p.Gly619=
NM_002693.3:c.1857C>G MANE Select	NP_002684.1:p.Gly619=