Canonical Allele Identifier: CA2630252694
Gene: POLG HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.89325705_89325708del , CM000677.2:g.89325705_89325708del GRCh38
NC_000015.9:g.89868936_89868939del , CM000677.1:g.89868936_89868939del GRCh37
NC_000015.8:g.87669940_87669943del NCBI36
NG_008218.1:g.14090_14093del
NG_008218.2:g.14090_14093del

Transcript Alleles

HGVS Amino-acid Change
ENST00000636937.2:c.1713-20_1713-17del ENSP00000516154.1:n.1713-20_1713-17del
ENST00000268124.11:c.1713-20_1713-17del MANE Select ENSP00000268124.5:n.1713-20_1713-17del
ENST00000530292.3:c.1314-20_1314-17del ENSP00000432885.2:n.1314-20_1314-17del
ENST00000635986.2:c.1713-20_1713-17del ENSP00000490653.2:n.1713-20_1713-17del
ENST00000636774.1:c.*280-20_*280-17del ENSP00000489799.1:n.*280-20_*280-17del
ENST00000637238.1:c.450-20_450-17del ENSP00000490756.1:n.450-20_450-17del
ENST00000637264.1:c.785-20_785-17del
ENST00000666746.1:c.1290-20_1290-17del
ENST00000670281.1:c.33-20_33-17del ENSP00000499709.1:n.33-20_33-17del
ENST00000672071.1:n.1911-20_1911-17del
ENST00000672923.2:n.1816-20_1816-17del
ENST00000268124.9:c.1713-20_1713-17del ENSP00000268124.5:n.1713-20_1713-17del
ENST00000442287.6:c.1713-20_1713-17del ENSP00000399851.2:n.1713-20_1713-17del
ENST00000526314.2:c.95-20_95-17del
ENST00000631044.2:c.*1096-20_*1096-17del ENSP00000486730.1:n.*1096-20_*1096-17del
NM_001126131.1:c.1713-20_1713-17del NP_001119603.1:n.1713-20_1713-17del
NM_002693.2:c.1713-20_1713-17del NP_002684.1:n.1713-20_1713-17del
NM_001126131.2:c.1713-20_1713-17del NP_001119603.1:n.1713-20_1713-17del
NM_002693.3:c.1713-20_1713-17del MANE Select NP_002684.1:n.1713-20_1713-17del