Canonical Allele Identifier: CA492288842

Gene: POLG

Linked Data

• MyVariant Identifiers: chr15:g.89861948C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.89318717C>T , CM000677.2:g.89318717C>T	GRCh38
NC_000015.9:g.89861948C>T , CM000677.1:g.89861948C>T	GRCh37
NC_000015.8:g.87662952C>T	NCBI36
NG_008218.1:g.21079G>A
NG_011736.1:g.79755C>T , LRG_500:g.79755C>T
NG_008218.2:g.21079G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000636937.2:c.3306G>A	ENSP00000516154.1:p.Gln1102=
ENST00000268124.11:c.3306G>A MANE Select	ENSP00000268124.5:p.Gln1102=
ENST00000530292.3:c.2907G>A	ENSP00000432885.2:p.Gln969=
ENST00000635986.2:c.*376G>A	ENSP00000490653.2:n.*376G>A
ENST00000636774.1:c.*1873G>A	ENSP00000489799.1:n.*1873G>A
ENST00000637238.1:c.2115G>A	ENSP00000490756.1:n.2115G>A
ENST00000637264.1:c.2378G>A
ENST00000666746.1:c.2883G>A
ENST00000672071.1:n.3504G>A
ENST00000672695.1:n.483G>A
ENST00000672923.2:n.3306G>A
ENST00000268124.9:c.3306G>A	ENSP00000268124.5:p.Gln1102=
ENST00000442287.6:c.3306G>A	ENSP00000399851.2:p.Gln1102=
ENST00000530292.2:c.390G>A	ENSP00000432885.1:p.Gln130=
ENST00000631044.2:c.*2730G>A	ENSP00000486730.1:n.*2730G>A
NM_001126131.1:c.3306G>A	NP_001119603.1:p.Gln1102=
NM_002693.2:c.3306G>A	NP_002684.1:p.Gln1102=
NM_001126131.2:c.3306G>A	NP_001119603.1:p.Gln1102=
NM_002693.3:c.3306G>A MANE Select	NP_002684.1:p.Gln1102=