Canonical Allele Identifier: CA619514141
Gene: POLG HGNC NCBI

Linked Data

dbSNP Id: rs1304536018

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.89325284_89325289del , CM000677.2:g.89325284_89325289del GRCh38
NC_000015.9:g.89868515_89868520del , CM000677.1:g.89868515_89868520del GRCh37
NC_000015.8:g.87669519_87669524del NCBI36
NG_008218.1:g.14512_14517del
NG_008218.2:g.14512_14517del

Transcript Alleles

HGVS Amino-acid Change
ENST00000636937.2:c.1949+166_1949+171del ENSP00000516154.1:n.1949+166_1949+171del
ENST00000268124.11:c.1949+166_1949+171del MANE Select ENSP00000268124.5:n.1949+166_1949+171del
ENST00000530292.3:c.1550+166_1550+171del ENSP00000432885.2:n.1550+166_1550+171del
ENST00000635986.2:c.1949+166_1949+171del ENSP00000490653.2:n.1949+166_1949+171del
ENST00000636774.1:c.*516+166_*516+171del ENSP00000489799.1:n.*516+166_*516+171del
ENST00000637238.1:c.646+206_646+211del ENSP00000490756.1:n.646+206_646+211del
ENST00000637264.1:c.1021+166_1021+171del
ENST00000666746.1:c.1526+166_1526+171del
ENST00000670281.1:c.269+166_269+171del ENSP00000499709.1:n.269+166_269+171del
ENST00000672071.1:n.2147+166_2147+171del
ENST00000672923.2:n.2052+166_2052+171del
ENST00000268124.9:c.1949+166_1949+171del ENSP00000268124.5:n.1949+166_1949+171del
ENST00000442287.6:c.1949+166_1949+171del ENSP00000399851.2:n.1949+166_1949+171del
ENST00000526314.2:c.331+166_331+171del
ENST00000526398.1:c.138+166_138+171del
ENST00000526573.1:n.35+166_35+171del
ENST00000532584.5:n.151+166_151+171del
ENST00000631044.2:c.*1332+166_*1332+171del ENSP00000486730.1:n.*1332+166_*1332+171del
NM_001126131.1:c.1949+166_1949+171del NP_001119603.1:n.1949+166_1949+171del
NM_002693.2:c.1949+166_1949+171del NP_002684.1:n.1949+166_1949+171del
NM_001126131.2:c.1949+166_1949+171del NP_001119603.1:n.1949+166_1949+171del
NM_002693.3:c.1949+166_1949+171del MANE Select NP_002684.1:n.1949+166_1949+171del