Canonical Allele Identifier: CA492078486

Gene: POLG

Linked Data

• MyVariant Identifiers: chr15:g.89872294G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.89329063G>A , CM000677.2:g.89329063G>A	GRCh38
NC_000015.9:g.89872294G>A , CM000677.1:g.89872294G>A	GRCh37
NC_000015.8:g.87673298G>A	NCBI36
NG_008218.1:g.10733C>T
NG_008218.2:g.10733C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000636937.2:c.903C>T	ENSP00000516154.1:p.Ile301=
ENST00000268124.11:c.903C>T MANE Select	ENSP00000268124.5:p.Ile301=
ENST00000530292.3:c.504C>T	ENSP00000432885.2:p.Ile168=
ENST00000635986.2:c.903C>T	ENSP00000490653.2:p.Ile301=
ENST00000636774.1:c.903C>T	ENSP00000489799.1:p.Ile301=
ENST00000666746.1:c.560C>T
ENST00000672071.1:n.1101C>T
ENST00000268124.9:c.903C>T	ENSP00000268124.5:p.Ile301=
ENST00000442287.6:c.903C>T	ENSP00000399851.2:p.Ile301=
ENST00000631044.2:c.*286C>T	ENSP00000486730.1:n.*286C>T
NM_001126131.1:c.903C>T	NP_001119603.1:p.Ile301=
NM_002693.2:c.903C>T	NP_002684.1:p.Ile301=
NM_001126131.2:c.903C>T	NP_001119603.1:p.Ile301=
NM_002693.3:c.903C>T MANE Select	NP_002684.1:p.Ile301=