Canonical Allele Identifier: CA2805170447
Gene: POLG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.89325753_89325754insACA , CM000677.2:g.89325753_89325754insACA GRCh38
NC_000015.9:g.89868984_89868985insACA , CM000677.1:g.89868984_89868985insACA GRCh37
NC_000015.8:g.87669988_87669989insACA NCBI36
NG_008218.1:g.14042_14043insTGT
NG_008218.2:g.14042_14043insTGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000636937.2:c.1713-68_1713-67insTGT ENSP00000516154.1:n.1713-68_1713-67insTGT
ENST00000268124.11:c.1713-68_1713-67insTGT MANE Select ENSP00000268124.5:n.1713-68_1713-67insTGT
ENST00000530292.3:c.1314-68_1314-67insTGT ENSP00000432885.2:n.1314-68_1314-67insTGT
ENST00000635986.2:c.1713-68_1713-67insTGT ENSP00000490653.2:n.1713-68_1713-67insTGT
ENST00000636774.1:c.*280-68_*280-67insTGT ENSP00000489799.1:n.*280-68_*280-67insTGT
ENST00000637238.1:c.450-68_450-67insTGT ENSP00000490756.1:n.450-68_450-67insTGT
ENST00000637264.1:c.785-68_785-67insTGT
ENST00000666746.1:c.1290-68_1290-67insTGT
ENST00000670281.1:c.33-68_33-67insTGT ENSP00000499709.1:n.33-68_33-67insTGT
ENST00000672071.1:n.1911-68_1911-67insTGT
ENST00000672923.2:n.1816-68_1816-67insTGT
ENST00000268124.9:c.1713-68_1713-67insTGT ENSP00000268124.5:n.1713-68_1713-67insTGT
ENST00000442287.6:c.1713-68_1713-67insTGT ENSP00000399851.2:n.1713-68_1713-67insTGT
ENST00000526314.2:c.95-68_95-67insTGT
ENST00000631044.2:c.*1096-68_*1096-67insTGT ENSP00000486730.1:n.*1096-68_*1096-67insTGT
NM_001126131.1:c.1713-68_1713-67insTGT NP_001119603.1:n.1713-68_1713-67insTGT
NM_002693.2:c.1713-68_1713-67insTGT NP_002684.1:n.1713-68_1713-67insTGT
NM_001126131.2:c.1713-68_1713-67insTGT NP_001119603.1:n.1713-68_1713-67insTGT
NM_002693.3:c.1713-68_1713-67insTGT MANE Select NP_002684.1:n.1713-68_1713-67insTGT