Canonical Allele Identifier: CA492289553

Gene: POLG

Linked Data

• MyVariant Identifiers: chr15:g.89868917T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.89325686T>G , CM000677.2:g.89325686T>G	GRCh38
NC_000015.9:g.89868917T>G , CM000677.1:g.89868917T>G	GRCh37
NC_000015.8:g.87669921T>G	NCBI36
NG_008218.1:g.14110A>C
NG_008218.2:g.14110A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000636937.2:c.1713A>C	ENSP00000516154.1:p.Gly571=
ENST00000268124.11:c.1713A>C MANE Select	ENSP00000268124.5:p.Gly571=
ENST00000530292.3:c.1314A>C	ENSP00000432885.2:p.Gly438=
ENST00000635986.2:c.1713A>C	ENSP00000490653.2:p.Gly571=
ENST00000636774.1:c.*280A>C	ENSP00000489799.1:n.*280A>C
ENST00000637238.1:c.450A>C	ENSP00000490756.1:p.Gly150=
ENST00000637264.1:c.785A>C
ENST00000666746.1:c.1290A>C
ENST00000670281.1:c.33A>C	ENSP00000499709.1:p.Gly11=
ENST00000672071.1:n.1911A>C
ENST00000672923.2:n.1816A>C
ENST00000268124.9:c.1713A>C	ENSP00000268124.5:p.Gly571=
ENST00000442287.6:c.1713A>C	ENSP00000399851.2:p.Gly571=
ENST00000526314.2:c.95A>C
ENST00000631044.2:c.*1096A>C	ENSP00000486730.1:n.*1096A>C
NM_001126131.1:c.1713A>C	NP_001119603.1:p.Gly571=
NM_002693.2:c.1713A>C	NP_002684.1:p.Gly571=
NM_001126131.2:c.1713A>C	NP_001119603.1:p.Gly571=
NM_002693.3:c.1713A>C MANE Select	NP_002684.1:p.Gly571=