Canonical Allele Identifier: CA492076484

Gene: POLG

Linked Data

• MyVariant Identifiers: chr15:g.89866689T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.89323458T>A , CM000677.2:g.89323458T>A	GRCh38
NC_000015.9:g.89866689T>A , CM000677.1:g.89866689T>A	GRCh37
NC_000015.8:g.87667693T>A	NCBI36
NG_008218.1:g.16338A>T
NG_008218.2:g.16338A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000636937.2:c.2211A>T	ENSP00000516154.1:p.Gly737=
ENST00000268124.11:c.2211A>T MANE Select	ENSP00000268124.5:p.Gly737=
ENST00000530292.3:c.1812A>T	ENSP00000432885.2:p.Gly604=
ENST00000635986.2:c.2211A>T	ENSP00000490653.2:p.Gly737=
ENST00000636774.1:c.*778A>T	ENSP00000489799.1:n.*778A>T
ENST00000637238.1:c.908A>T	ENSP00000490756.1:n.908A>T
ENST00000637264.1:c.1283A>T
ENST00000666746.1:c.1788A>T
ENST00000670281.1:c.531A>T	ENSP00000499709.1:p.Gly177=
ENST00000672071.1:n.2409A>T
ENST00000672923.2:n.2314A>T
ENST00000268124.9:c.2211A>T	ENSP00000268124.5:p.Gly737=
ENST00000442287.6:c.2211A>T	ENSP00000399851.2:p.Gly737=
ENST00000526314.2:c.539+357A>T
ENST00000526398.1:c.360A>T
ENST00000532584.5:n.413A>T
ENST00000631044.2:c.*1635A>T	ENSP00000486730.1:n.*1635A>T
NM_001126131.1:c.2211A>T	NP_001119603.1:p.Gly737=
NM_002693.2:c.2211A>T	NP_002684.1:p.Gly737=
NM_001126131.2:c.2211A>T	NP_001119603.1:p.Gly737=
NM_002693.3:c.2211A>T MANE Select	NP_002684.1:p.Gly737=