Canonical Allele Identifier: CA2805170456
Gene: POLG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.89325760_89325761insC , CM000677.2:g.89325760_89325761insC GRCh38
NC_000015.9:g.89868991_89868992insC , CM000677.1:g.89868991_89868992insC GRCh37
NC_000015.8:g.87669995_87669996insC NCBI36
NG_008218.1:g.14035_14036insG
NG_008218.2:g.14035_14036insG

Transcript Alleles

HGVS Amino-acid Change
ENST00000636937.2:c.1713-75_1713-74insG ENSP00000516154.1:n.1713-75_1713-74insG
ENST00000268124.11:c.1713-75_1713-74insG MANE Select ENSP00000268124.5:n.1713-75_1713-74insG
ENST00000530292.3:c.1314-75_1314-74insG ENSP00000432885.2:n.1314-75_1314-74insG
ENST00000635986.2:c.1713-75_1713-74insG ENSP00000490653.2:n.1713-75_1713-74insG
ENST00000636774.1:c.*280-75_*280-74insG ENSP00000489799.1:n.*280-75_*280-74insG
ENST00000637238.1:c.450-75_450-74insG ENSP00000490756.1:n.450-75_450-74insG
ENST00000637264.1:c.785-75_785-74insG
ENST00000666746.1:c.1290-75_1290-74insG
ENST00000670281.1:c.33-75_33-74insG ENSP00000499709.1:n.33-75_33-74insG
ENST00000672071.1:n.1911-75_1911-74insG
ENST00000672923.2:n.1816-75_1816-74insG
ENST00000268124.9:c.1713-75_1713-74insG ENSP00000268124.5:n.1713-75_1713-74insG
ENST00000442287.6:c.1713-75_1713-74insG ENSP00000399851.2:n.1713-75_1713-74insG
ENST00000526314.2:c.95-75_95-74insG
ENST00000631044.2:c.*1096-75_*1096-74insG ENSP00000486730.1:n.*1096-75_*1096-74insG
NM_001126131.1:c.1713-75_1713-74insG NP_001119603.1:n.1713-75_1713-74insG
NM_002693.2:c.1713-75_1713-74insG NP_002684.1:n.1713-75_1713-74insG
NM_001126131.2:c.1713-75_1713-74insG NP_001119603.1:n.1713-75_1713-74insG
NM_002693.3:c.1713-75_1713-74insG MANE Select NP_002684.1:n.1713-75_1713-74insG