Canonical Allele Identifier: CA716909907

Gene: POLG

Linked Data

• dbSNP Id: rs71149294
• MyVariant Identifiers: chr15:g.89868528_89868529insGAGGGTGTGTGTGT (hg19) ; chr15:g.89325297_89325298insGAGGGTGTGTGTGT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.89325298_89325299insAGGGTGTGTGTGTG , CM000677.2:g.89325298_89325299insAGGGTGTGTGTGTG	GRCh38
NC_000015.9:g.89868529_89868530insAGGGTGTGTGTGTG , CM000677.1:g.89868529_89868530insAGGGTGTGTGTGTG	GRCh37
NC_000015.8:g.87669533_87669534insAGGGTGTGTGTGTG	NCBI36
NG_008218.1:g.14498_14499insACACACACACCCTC
NG_008218.2:g.14498_14499insACACACACACCCTC

Transcript Alleles

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