Canonical Allele Identifier: CA492076533

Gene: POLG

Linked Data

• MyVariant Identifiers: chr15:g.89866704A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.89323473A>G , CM000677.2:g.89323473A>G	GRCh38
NC_000015.9:g.89866704A>G , CM000677.1:g.89866704A>G	GRCh37
NC_000015.8:g.87667708A>G	NCBI36
NG_008218.1:g.16323T>C
NG_008218.2:g.16323T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000636937.2:c.2196T>C	ENSP00000516154.1:p.Tyr732=
ENST00000268124.11:c.2196T>C MANE Select	ENSP00000268124.5:p.Tyr732=
ENST00000530292.3:c.1797T>C	ENSP00000432885.2:p.Tyr599=
ENST00000635986.2:c.2196T>C	ENSP00000490653.2:p.Tyr732=
ENST00000636774.1:c.*763T>C	ENSP00000489799.1:n.*763T>C
ENST00000637238.1:c.893T>C	ENSP00000490756.1:n.893T>C
ENST00000637264.1:c.1268T>C
ENST00000666746.1:c.1773T>C
ENST00000670281.1:c.516T>C	ENSP00000499709.1:p.Tyr172=
ENST00000672071.1:n.2394T>C
ENST00000672923.2:n.2299T>C
ENST00000268124.9:c.2196T>C	ENSP00000268124.5:p.Tyr732=
ENST00000442287.6:c.2196T>C	ENSP00000399851.2:p.Tyr732=
ENST00000526314.2:c.539+342T>C
ENST00000526398.1:c.345T>C
ENST00000532584.5:n.398T>C
ENST00000631044.2:c.*1620T>C	ENSP00000486730.1:n.*1620T>C
NM_001126131.1:c.2196T>C	NP_001119603.1:p.Tyr732=
NM_002693.2:c.2196T>C	NP_002684.1:p.Tyr732=
NM_001126131.2:c.2196T>C	NP_001119603.1:p.Tyr732=
NM_002693.3:c.2196T>C MANE Select	NP_002684.1:p.Tyr732=