Canonical Allele Identifier: CA972587425
Gene: POLG HGNC NCBI

Linked Data

dbSNP Id: rs2055473097

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.89325127_89325280del , CM000677.2:g.89325127_89325280del GRCh38
NC_000015.9:g.89868358_89868511del , CM000677.1:g.89868358_89868511del GRCh37
NC_000015.8:g.87669362_87669515del NCBI36
NG_008218.1:g.14519_14672del
NG_008218.2:g.14519_14672del

Transcript Alleles

HGVS Amino-acid Change
ENST00000636937.2:c.1949+173_1949+326del ENSP00000516154.1:n.1949+173_1949+326del
ENST00000268124.11:c.1949+173_1949+326del MANE Select ENSP00000268124.5:n.1949+173_1949+326del
ENST00000530292.3:c.1550+173_1550+326del ENSP00000432885.2:n.1550+173_1550+326del
ENST00000635986.2:c.1949+173_1949+326del ENSP00000490653.2:n.1949+173_1949+326del
ENST00000636774.1:c.*516+173_*516+326del ENSP00000489799.1:n.*516+173_*516+326del
ENST00000637238.1:c.646+213_646+366del ENSP00000490756.1:n.646+213_646+366del
ENST00000637264.1:c.1021+173_1021+326del
ENST00000666746.1:c.1526+173_1526+326del
ENST00000670281.1:c.269+173_269+326del ENSP00000499709.1:n.269+173_269+326del
ENST00000672071.1:n.2147+173_2147+326del
ENST00000672923.2:n.2052+173_2052+326del
ENST00000268124.9:c.1949+173_1949+326del ENSP00000268124.5:n.1949+173_1949+326del
ENST00000442287.6:c.1949+173_1949+326del ENSP00000399851.2:n.1949+173_1949+326del
ENST00000526314.2:c.331+173_331+326del
ENST00000526398.1:c.138+173_138+326del
ENST00000526573.1:n.35+173_35+326del
ENST00000532584.5:n.151+173_151+326del
ENST00000631044.2:c.*1332+173_*1332+326del ENSP00000486730.1:n.*1332+173_*1332+326del
NM_001126131.1:c.1949+173_1949+326del NP_001119603.1:n.1949+173_1949+326del
NM_002693.2:c.1949+173_1949+326del NP_002684.1:n.1949+173_1949+326del
NM_001126131.2:c.1949+173_1949+326del NP_001119603.1:n.1949+173_1949+326del
NM_002693.3:c.1949+173_1949+326del MANE Select NP_002684.1:n.1949+173_1949+326del