Canonical Allele Identifier: CA2597948980
Gene: POLG HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.89325203_89325278del , CM000677.2:g.89325203_89325278del GRCh38
NC_000015.9:g.89868434_89868509del , CM000677.1:g.89868434_89868509del GRCh37
NC_000015.8:g.87669438_87669513del NCBI36
NG_008218.1:g.14521_14596del
NG_008218.2:g.14521_14596del

Transcript Alleles

HGVS Amino-acid Change
ENST00000636937.2:c.1949+175_1949+250del ENSP00000516154.1:n.1949+175_1949+250del
ENST00000268124.11:c.1949+175_1949+250del MANE Select ENSP00000268124.5:n.1949+175_1949+250del
ENST00000530292.3:c.1550+175_1550+250del ENSP00000432885.2:n.1550+175_1550+250del
ENST00000635986.2:c.1949+175_1949+250del ENSP00000490653.2:n.1949+175_1949+250del
ENST00000636774.1:c.*516+175_*516+250del ENSP00000489799.1:n.*516+175_*516+250del
ENST00000637238.1:c.646+215_646+290del ENSP00000490756.1:n.646+215_646+290del
ENST00000637264.1:c.1021+175_1021+250del
ENST00000666746.1:c.1526+175_1526+250del
ENST00000670281.1:c.269+175_269+250del ENSP00000499709.1:n.269+175_269+250del
ENST00000672071.1:n.2147+175_2147+250del
ENST00000672923.2:n.2052+175_2052+250del
ENST00000268124.9:c.1949+175_1949+250del ENSP00000268124.5:n.1949+175_1949+250del
ENST00000442287.6:c.1949+175_1949+250del ENSP00000399851.2:n.1949+175_1949+250del
ENST00000526314.2:c.331+175_331+250del
ENST00000526398.1:c.138+175_138+250del
ENST00000526573.1:n.35+175_35+250del
ENST00000532584.5:n.151+175_151+250del
ENST00000631044.2:c.*1332+175_*1332+250del ENSP00000486730.1:n.*1332+175_*1332+250del
NM_001126131.1:c.1949+175_1949+250del NP_001119603.1:n.1949+175_1949+250del
NM_002693.2:c.1949+175_1949+250del NP_002684.1:n.1949+175_1949+250del
NM_001126131.2:c.1949+175_1949+250del NP_001119603.1:n.1949+175_1949+250del
NM_002693.3:c.1949+175_1949+250del MANE Select NP_002684.1:n.1949+175_1949+250del