Canonical Allele Identifier: CA972590079
Gene: POLG HGNC NCBI

Linked Data

dbSNP Id: rs2055498559

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.89325299_89325300insT , CM000677.2:g.89325299_89325300insT GRCh38
NC_000015.9:g.89868530_89868531insT , CM000677.1:g.89868530_89868531insT GRCh37
NC_000015.8:g.87669534_87669535insT NCBI36
NG_008218.1:g.14496_14497insA
NG_008218.2:g.14496_14497insA

Transcript Alleles

HGVS Amino-acid Change
ENST00000636937.2:c.1949+150_1949+151insA ENSP00000516154.1:n.1949+150_1949+151insA
ENST00000268124.11:c.1949+150_1949+151insA MANE Select ENSP00000268124.5:n.1949+150_1949+151insA
ENST00000530292.3:c.1550+150_1550+151insA ENSP00000432885.2:n.1550+150_1550+151insA
ENST00000635986.2:c.1949+150_1949+151insA ENSP00000490653.2:n.1949+150_1949+151insA
ENST00000636774.1:c.*516+150_*516+151insA ENSP00000489799.1:n.*516+150_*516+151insA
ENST00000637238.1:c.646+190_646+191insA ENSP00000490756.1:n.646+190_646+191insA
ENST00000637264.1:c.1021+150_1021+151insA
ENST00000666746.1:c.1526+150_1526+151insA
ENST00000670281.1:c.269+150_269+151insA ENSP00000499709.1:n.269+150_269+151insA
ENST00000672071.1:n.2147+150_2147+151insA
ENST00000672923.2:n.2052+150_2052+151insA
ENST00000268124.9:c.1949+150_1949+151insA ENSP00000268124.5:n.1949+150_1949+151insA
ENST00000442287.6:c.1949+150_1949+151insA ENSP00000399851.2:n.1949+150_1949+151insA
ENST00000526314.2:c.331+150_331+151insA
ENST00000526398.1:c.138+150_138+151insA
ENST00000526573.1:n.35+150_35+151insA
ENST00000532584.5:n.151+150_151+151insA
ENST00000631044.2:c.*1332+150_*1332+151insA ENSP00000486730.1:n.*1332+150_*1332+151insA
NM_001126131.1:c.1949+150_1949+151insA NP_001119603.1:n.1949+150_1949+151insA
NM_002693.2:c.1949+150_1949+151insA NP_002684.1:n.1949+150_1949+151insA
NM_001126131.2:c.1949+150_1949+151insA NP_001119603.1:n.1949+150_1949+151insA
NM_002693.3:c.1949+150_1949+151insA MANE Select NP_002684.1:n.1949+150_1949+151insA