Canonical Allele Identifier: CA2630251940
Gene: POLG HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.89325304_89325305insCG , CM000677.2:g.89325304_89325305insCG GRCh38
NC_000015.9:g.89868535_89868536insCG , CM000677.1:g.89868535_89868536insCG GRCh37
NC_000015.8:g.87669539_87669540insCG NCBI36
NG_008218.1:g.14492_14493insGC
NG_008218.2:g.14492_14493insGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000636937.2:c.1949+146_1949+147insGC ENSP00000516154.1:n.1949+146_1949+147insGC
ENST00000268124.11:c.1949+146_1949+147insGC MANE Select ENSP00000268124.5:n.1949+146_1949+147insGC
ENST00000530292.3:c.1550+146_1550+147insGC ENSP00000432885.2:n.1550+146_1550+147insGC
ENST00000635986.2:c.1949+146_1949+147insGC ENSP00000490653.2:n.1949+146_1949+147insGC
ENST00000636774.1:c.*516+146_*516+147insGC ENSP00000489799.1:n.*516+146_*516+147insGC
ENST00000637238.1:c.646+186_646+187insGC ENSP00000490756.1:n.646+186_646+187insGC
ENST00000637264.1:c.1021+146_1021+147insGC
ENST00000666746.1:c.1526+146_1526+147insGC
ENST00000670281.1:c.269+146_269+147insGC ENSP00000499709.1:n.269+146_269+147insGC
ENST00000672071.1:n.2147+146_2147+147insGC
ENST00000672923.2:n.2052+146_2052+147insGC
ENST00000268124.9:c.1949+146_1949+147insGC ENSP00000268124.5:n.1949+146_1949+147insGC
ENST00000442287.6:c.1949+146_1949+147insGC ENSP00000399851.2:n.1949+146_1949+147insGC
ENST00000526314.2:c.331+146_331+147insGC
ENST00000526398.1:c.138+146_138+147insGC
ENST00000526573.1:n.35+146_35+147insGC
ENST00000532584.5:n.151+146_151+147insGC
ENST00000631044.2:c.*1332+146_*1332+147insGC ENSP00000486730.1:n.*1332+146_*1332+147insGC
NM_001126131.1:c.1949+146_1949+147insGC NP_001119603.1:n.1949+146_1949+147insGC
NM_002693.2:c.1949+146_1949+147insGC NP_002684.1:n.1949+146_1949+147insGC
NM_001126131.2:c.1949+146_1949+147insGC NP_001119603.1:n.1949+146_1949+147insGC
NM_002693.3:c.1949+146_1949+147insGC MANE Select NP_002684.1:n.1949+146_1949+147insGC