Canonical Allele Identifier: CA492076555

Gene: POLG

Linked Data

• MyVariant Identifiers: chr15:g.89866716G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.89323485G>T , CM000677.2:g.89323485G>T	GRCh38
NC_000015.9:g.89866716G>T , CM000677.1:g.89866716G>T	GRCh37
NC_000015.8:g.87667720G>T	NCBI36
NG_008218.1:g.16311C>A
NG_008218.2:g.16311C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000636937.2:c.2184C>A	ENSP00000516154.1:p.Thr728=
ENST00000268124.11:c.2184C>A MANE Select	ENSP00000268124.5:p.Thr728=
ENST00000530292.3:c.1785C>A	ENSP00000432885.2:p.Thr595=
ENST00000635986.2:c.2184C>A	ENSP00000490653.2:p.Thr728=
ENST00000636774.1:c.*751C>A	ENSP00000489799.1:n.*751C>A
ENST00000637238.1:c.881C>A	ENSP00000490756.1:n.881C>A
ENST00000637264.1:c.1256C>A
ENST00000666746.1:c.1761C>A
ENST00000670281.1:c.504C>A	ENSP00000499709.1:p.Thr168=
ENST00000672071.1:n.2382C>A
ENST00000672923.2:n.2287C>A
ENST00000268124.9:c.2184C>A	ENSP00000268124.5:p.Thr728=
ENST00000442287.6:c.2184C>A	ENSP00000399851.2:p.Thr728=
ENST00000526314.2:c.539+330C>A
ENST00000526398.1:c.333C>A
ENST00000532584.5:n.386C>A
ENST00000631044.2:c.*1608C>A	ENSP00000486730.1:n.*1608C>A
NM_001126131.1:c.2184C>A	NP_001119603.1:p.Thr728=
NM_002693.2:c.2184C>A	NP_002684.1:p.Thr728=
NM_001126131.2:c.2184C>A	NP_001119603.1:p.Thr728=
NM_002693.3:c.2184C>A MANE Select	NP_002684.1:p.Thr728=