Canonical Allele Identifier: CA2580090393
Gene: POLG HGNC NCBI
POLGARF HGNC NCBI

Linked Data

ClinVar Variation Id: 1767733
ClinVar RCV Id: RCV002386974

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.89333618_89333627delinsC , CM000677.2:g.89333618_89333627delinsC GRCh38
NC_000015.9:g.89876849_89876858delinsC , CM000677.1:g.89876849_89876858delinsC GRCh37
NC_000015.8:g.87677853_87677862delinsC NCBI36
NG_008218.1:g.6169_6178delinsG
NG_008218.2:g.6169_6178delinsG

Transcript Alleles

HGVS Amino-acid change
ENST00000636937.2:c.128_137delinsG (POLG) ENSP00000516154.1:p.Gln43_Gln46delinsArg
ENST00000706918.1:c.183_192delinsG (POLGARF) ENSP00000516626.1:p.Ala62_Ala64del
ENST00000268124.11:c.128_137delinsG (POLG) MANE Select ENSP00000268124.5:p.Gln43_Gln46delinsArg
ENST00000635986.2:c.128_137delinsG (POLG) ENSP00000490653.2:p.Gln43_Gln46delinsArg
ENST00000636774.1:c.128_137delinsG (POLG) ENSP00000489799.1:p.Gln43_Gln46delinsArg
ENST00000650303.2:c.183_192delinsG (POLG) ENSP00000497242.2:p.Ala62_Ala64del
ENST00000672071.1:n.326_335delinsG (POLG)
ENST00000268124.9:c.128_137delinsG (POLG) ENSP00000268124.5:p.Gln43_Gln46delinsArg
ENST00000442287.6:c.128_137delinsG (POLG) ENSP00000399851.2:p.Gln43_Gln46delinsArg
ENST00000631044.2:c.128_137delinsG (POLG) ENSP00000486730.1:p.Gln43_Gln46delinsArg
NM_001126131.1:c.128_137delinsG (POLG) NP_001119603.1:p.Gln43_Gln46delinsArg
NM_002693.2:c.128_137delinsG (POLG) NP_002684.1:p.Gln43_Gln46delinsArg
NM_001126131.2:c.128_137delinsG (POLG) NP_001119603.1:p.Gln43_Gln46delinsArg
NM_002693.3:c.128_137delinsG (POLG) MANE Select NP_002684.1:p.Gln43_Gln46delinsArg