Canonical Allele Identifier: CA393767230
Gene: POLG HGNC NCBI
POLGARF HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.89330248C>T , CM000677.2:g.89330248C>T GRCh38
NC_000015.9:g.89873479C>T , CM000677.1:g.89873479C>T GRCh37
NC_000015.8:g.87674483C>T NCBI36
NG_008218.1:g.9548G>A
NG_008218.2:g.9548G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000636937.2:c.688G>A (POLG) ENSP00000516154.1:p.Glu230Lys
ENST00000706918.1:c.743G>A (POLGARF) ENSP00000516626.1:p.Gly248Glu
ENST00000268124.11:c.688G>A (POLG) MANE Select ENSP00000268124.5:p.Glu230Lys
ENST00000530292.3:c.289G>A (POLG) ENSP00000432885.2:p.Glu97Lys
ENST00000635986.2:c.688G>A (POLG) ENSP00000490653.2:p.Glu230Lys
ENST00000636774.1:c.688G>A (POLG) ENSP00000489799.1:p.Glu230Lys
ENST00000637307.1:c.63G>A (POLG)
ENST00000650303.2:c.743G>A (POLG) ENSP00000497242.2:p.Gly248Glu
ENST00000666746.1:c.345G>A (POLG)
ENST00000672071.1:n.886G>A (POLG)
ENST00000268124.9:c.688G>A (POLG) ENSP00000268124.5:p.Glu230Lys
ENST00000442287.6:c.688G>A (POLG) ENSP00000399851.2:p.Glu230Lys
ENST00000631044.2:c.*71G>A (POLG) ENSP00000486730.1:n.*71G>A
NM_001126131.1:c.688G>A (POLG) NP_001119603.1:p.Glu230Lys
NM_002693.2:c.688G>A (POLG) NP_002684.1:p.Glu230Lys
NM_001126131.2:c.688G>A (POLG) NP_001119603.1:p.Glu230Lys
NM_002693.3:c.688G>A (POLG) MANE Select NP_002684.1:p.Glu230Lys