Canonical Allele Identifier: CA492289544

Gene: POLG

Linked Data

• MyVariant Identifiers: chr15:g.89870162A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.89326931A>T , CM000677.2:g.89326931A>T	GRCh38
NC_000015.9:g.89870162A>T , CM000677.1:g.89870162A>T	GRCh37
NC_000015.8:g.87671166A>T	NCBI36
NG_008218.1:g.12865T>A
NG_008218.2:g.12865T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000636937.2:c.1566T>A	ENSP00000516154.1:p.Gly522=
ENST00000268124.11:c.1566T>A MANE Select	ENSP00000268124.5:p.Gly522=
ENST00000530292.3:c.1167T>A	ENSP00000432885.2:p.Gly389=
ENST00000635986.2:c.1566T>A	ENSP00000490653.2:p.Gly522=
ENST00000636774.1:c.*133T>A	ENSP00000489799.1:n.*133T>A
ENST00000637238.1:c.303T>A	ENSP00000490756.1:p.Gly101=
ENST00000637264.1:c.638T>A
ENST00000666746.1:c.1143T>A
ENST00000672071.1:n.1764T>A
ENST00000672923.2:n.1669T>A
ENST00000268124.9:c.1566T>A	ENSP00000268124.5:p.Gly522=
ENST00000442287.6:c.1566T>A	ENSP00000399851.2:p.Gly522=
ENST00000631044.2:c.*949T>A	ENSP00000486730.1:n.*949T>A
NM_001126131.1:c.1566T>A	NP_001119603.1:p.Gly522=
NM_002693.2:c.1566T>A	NP_002684.1:p.Gly522=
NM_001126131.2:c.1566T>A	NP_001119603.1:p.Gly522=
NM_002693.3:c.1566T>A MANE Select	NP_002684.1:p.Gly522=