Canonical Allele Identifier: CA716909886
Gene: POLG HGNC NCBI

Linked Data

dbSNP Id: rs1324166758

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.89325295_89325296insCA , CM000677.2:g.89325295_89325296insCA GRCh38
NC_000015.9:g.89868526_89868527insCA , CM000677.1:g.89868526_89868527insCA GRCh37
NC_000015.8:g.87669530_87669531insCA NCBI36
NG_008218.1:g.14501_14502insGT
NG_008218.2:g.14501_14502insGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000636937.2:c.1949+155_1949+156insGT ENSP00000516154.1:n.1949+155_1949+156insGT
ENST00000268124.11:c.1949+155_1949+156insGT MANE Select ENSP00000268124.5:n.1949+155_1949+156insGT
ENST00000530292.3:c.1550+155_1550+156insGT ENSP00000432885.2:n.1550+155_1550+156insGT
ENST00000635986.2:c.1949+155_1949+156insGT ENSP00000490653.2:n.1949+155_1949+156insGT
ENST00000636774.1:c.*516+155_*516+156insGT ENSP00000489799.1:n.*516+155_*516+156insGT
ENST00000637238.1:c.646+195_646+196insGT ENSP00000490756.1:n.646+195_646+196insGT
ENST00000637264.1:c.1021+155_1021+156insGT
ENST00000666746.1:c.1526+155_1526+156insGT
ENST00000670281.1:c.269+155_269+156insGT ENSP00000499709.1:n.269+155_269+156insGT
ENST00000672071.1:n.2147+155_2147+156insGT
ENST00000672923.2:n.2052+155_2052+156insGT
ENST00000268124.9:c.1949+155_1949+156insGT ENSP00000268124.5:n.1949+155_1949+156insGT
ENST00000442287.6:c.1949+155_1949+156insGT ENSP00000399851.2:n.1949+155_1949+156insGT
ENST00000526314.2:c.331+155_331+156insGT
ENST00000526398.1:c.138+155_138+156insGT
ENST00000526573.1:n.35+155_35+156insGT
ENST00000532584.5:n.151+155_151+156insGT
ENST00000631044.2:c.*1332+155_*1332+156insGT ENSP00000486730.1:n.*1332+155_*1332+156insGT
NM_001126131.1:c.1949+155_1949+156insGT NP_001119603.1:n.1949+155_1949+156insGT
NM_002693.2:c.1949+155_1949+156insGT NP_002684.1:n.1949+155_1949+156insGT
NM_001126131.2:c.1949+155_1949+156insGT NP_001119603.1:n.1949+155_1949+156insGT
NM_002693.3:c.1949+155_1949+156insGT MANE Select NP_002684.1:n.1949+155_1949+156insGT