Canonical Allele Identifier: CA716909919
Gene: POLG HGNC NCBI

Linked Data

dbSNP Id: rs71149294

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.89325298_89325299insAGGGTG , CM000677.2:g.89325298_89325299insAGGGTG GRCh38
NC_000015.9:g.89868529_89868530insAGGGTG , CM000677.1:g.89868529_89868530insAGGGTG GRCh37
NC_000015.8:g.87669533_87669534insAGGGTG NCBI36
NG_008218.1:g.14498_14499insACCCTC
NG_008218.2:g.14498_14499insACCCTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000636937.2:c.1949+152_1949+153insACCCTC ENSP00000516154.1:n.1949+152_1949+153insACCCTC
ENST00000268124.11:c.1949+152_1949+153insACCCTC MANE Select ENSP00000268124.5:n.1949+152_1949+153insACCCTC
ENST00000530292.3:c.1550+152_1550+153insACCCTC ENSP00000432885.2:n.1550+152_1550+153insACCCTC
ENST00000635986.2:c.1949+152_1949+153insACCCTC ENSP00000490653.2:n.1949+152_1949+153insACCCTC
ENST00000636774.1:c.*516+152_*516+153insACCCTC ENSP00000489799.1:n.*516+152_*516+153insACCCTC
ENST00000637238.1:c.646+192_646+193insACCCTC ENSP00000490756.1:n.646+192_646+193insACCCTC
ENST00000637264.1:c.1021+152_1021+153insACCCTC
ENST00000666746.1:c.1526+152_1526+153insACCCTC
ENST00000670281.1:c.269+152_269+153insACCCTC ENSP00000499709.1:n.269+152_269+153insACCCTC
ENST00000672071.1:n.2147+152_2147+153insACCCTC
ENST00000672923.2:n.2052+152_2052+153insACCCTC
ENST00000268124.9:c.1949+152_1949+153insACCCTC ENSP00000268124.5:n.1949+152_1949+153insACCCTC
ENST00000442287.6:c.1949+152_1949+153insACCCTC ENSP00000399851.2:n.1949+152_1949+153insACCCTC
ENST00000526314.2:c.331+152_331+153insACCCTC
ENST00000526398.1:c.138+152_138+153insACCCTC
ENST00000526573.1:n.35+152_35+153insACCCTC
ENST00000532584.5:n.151+152_151+153insACCCTC
ENST00000631044.2:c.*1332+152_*1332+153insACCCTC ENSP00000486730.1:n.*1332+152_*1332+153insACCCTC
NM_001126131.1:c.1949+152_1949+153insACCCTC NP_001119603.1:n.1949+152_1949+153insACCCTC
NM_002693.2:c.1949+152_1949+153insACCCTC NP_002684.1:n.1949+152_1949+153insACCCTC
NM_001126131.2:c.1949+152_1949+153insACCCTC NP_001119603.1:n.1949+152_1949+153insACCCTC
NM_002693.3:c.1949+152_1949+153insACCCTC MANE Select NP_002684.1:n.1949+152_1949+153insACCCTC