Canonical Allele Identifier: CA492076651

Gene: POLG

Linked Data

• MyVariant Identifiers: chr15:g.89866737G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.89323506G>T , CM000677.2:g.89323506G>T	GRCh38
NC_000015.9:g.89866737G>T , CM000677.1:g.89866737G>T	GRCh37
NC_000015.8:g.87667741G>T	NCBI36
NG_008218.1:g.16290C>A
NG_008218.2:g.16290C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000636937.2:c.2163C>A	ENSP00000516154.1:p.Ala721=
ENST00000268124.11:c.2163C>A MANE Select	ENSP00000268124.5:p.Ala721=
ENST00000530292.3:c.1764C>A	ENSP00000432885.2:p.Ala588=
ENST00000635986.2:c.2163C>A	ENSP00000490653.2:p.Ala721=
ENST00000636774.1:c.*730C>A	ENSP00000489799.1:n.*730C>A
ENST00000637238.1:c.860C>A	ENSP00000490756.1:n.860C>A
ENST00000637264.1:c.1235C>A
ENST00000666746.1:c.1740C>A
ENST00000670281.1:c.483C>A	ENSP00000499709.1:p.Ala161=
ENST00000672071.1:n.2361C>A
ENST00000672923.2:n.2266C>A
ENST00000268124.9:c.2163C>A	ENSP00000268124.5:p.Ala721=
ENST00000442287.6:c.2163C>A	ENSP00000399851.2:p.Ala721=
ENST00000526314.2:c.539+309C>A
ENST00000526398.1:c.312C>A
ENST00000532584.5:n.365C>A
ENST00000631044.2:c.*1587C>A	ENSP00000486730.1:n.*1587C>A
NM_001126131.1:c.2163C>A	NP_001119603.1:p.Ala721=
NM_002693.2:c.2163C>A	NP_002684.1:p.Ala721=
NM_001126131.2:c.2163C>A	NP_001119603.1:p.Ala721=
NM_002693.3:c.2163C>A MANE Select	NP_002684.1:p.Ala721=