Canonical Allele Identifier: CA972588751
Gene: POLG HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.89325199_89325278del , CM000677.2:g.89325199_89325278del GRCh38
NC_000015.9:g.89868430_89868509del , CM000677.1:g.89868430_89868509del GRCh37
NC_000015.8:g.87669434_87669513del NCBI36
NG_008218.1:g.14537_14616del
NG_008218.2:g.14537_14616del

Transcript Alleles

HGVS Amino-acid Change
ENST00000636937.2:c.1949+191_1949+270del ENSP00000516154.1:n.1949+191_1949+270del
ENST00000268124.11:c.1949+191_1949+270del MANE Select ENSP00000268124.5:n.1949+191_1949+270del
ENST00000530292.3:c.1550+191_1550+270del ENSP00000432885.2:n.1550+191_1550+270del
ENST00000635986.2:c.1949+191_1949+270del ENSP00000490653.2:n.1949+191_1949+270del
ENST00000636774.1:c.*516+191_*516+270del ENSP00000489799.1:n.*516+191_*516+270del
ENST00000637238.1:c.646+231_646+310del ENSP00000490756.1:n.646+231_646+310del
ENST00000637264.1:c.1021+191_1021+270del
ENST00000666746.1:c.1526+191_1526+270del
ENST00000670281.1:c.269+191_269+270del ENSP00000499709.1:n.269+191_269+270del
ENST00000672071.1:n.2147+191_2147+270del
ENST00000672923.2:n.2052+191_2052+270del
ENST00000268124.9:c.1949+191_1949+270del ENSP00000268124.5:n.1949+191_1949+270del
ENST00000442287.6:c.1949+191_1949+270del ENSP00000399851.2:n.1949+191_1949+270del
ENST00000526314.2:c.331+191_331+270del
ENST00000526398.1:c.138+191_138+270del
ENST00000526573.1:n.35+191_35+270del
ENST00000532584.5:n.151+191_151+270del
ENST00000631044.2:c.*1332+191_*1332+270del ENSP00000486730.1:n.*1332+191_*1332+270del
NM_001126131.1:c.1949+191_1949+270del NP_001119603.1:n.1949+191_1949+270del
NM_002693.2:c.1949+191_1949+270del NP_002684.1:n.1949+191_1949+270del
NM_001126131.2:c.1949+191_1949+270del NP_001119603.1:n.1949+191_1949+270del
NM_002693.3:c.1949+191_1949+270del MANE Select NP_002684.1:n.1949+191_1949+270del