Canonical Allele Identifier: CA972589964
Gene: POLG HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.89325282_89325288del , CM000677.2:g.89325282_89325288del GRCh38
NC_000015.9:g.89868513_89868519del , CM000677.1:g.89868513_89868519del GRCh37
NC_000015.8:g.87669517_87669523del NCBI36
NG_008218.1:g.14508_14514del
NG_008218.2:g.14508_14514del

Transcript Alleles

HGVS Amino-acid Change
ENST00000636937.2:c.1949+162_1949+168del ENSP00000516154.1:n.1949+162_1949+168del
ENST00000268124.11:c.1949+162_1949+168del MANE Select ENSP00000268124.5:n.1949+162_1949+168del
ENST00000530292.3:c.1550+162_1550+168del ENSP00000432885.2:n.1550+162_1550+168del
ENST00000635986.2:c.1949+162_1949+168del ENSP00000490653.2:n.1949+162_1949+168del
ENST00000636774.1:c.*516+162_*516+168del ENSP00000489799.1:n.*516+162_*516+168del
ENST00000637238.1:c.646+202_646+208del ENSP00000490756.1:n.646+202_646+208del
ENST00000637264.1:c.1021+162_1021+168del
ENST00000666746.1:c.1526+162_1526+168del
ENST00000670281.1:c.269+162_269+168del ENSP00000499709.1:n.269+162_269+168del
ENST00000672071.1:n.2147+162_2147+168del
ENST00000672923.2:n.2052+162_2052+168del
ENST00000268124.9:c.1949+162_1949+168del ENSP00000268124.5:n.1949+162_1949+168del
ENST00000442287.6:c.1949+162_1949+168del ENSP00000399851.2:n.1949+162_1949+168del
ENST00000526314.2:c.331+162_331+168del
ENST00000526398.1:c.138+162_138+168del
ENST00000526573.1:n.35+162_35+168del
ENST00000532584.5:n.151+162_151+168del
ENST00000631044.2:c.*1332+162_*1332+168del ENSP00000486730.1:n.*1332+162_*1332+168del
NM_001126131.1:c.1949+162_1949+168del NP_001119603.1:n.1949+162_1949+168del
NM_002693.2:c.1949+162_1949+168del NP_002684.1:n.1949+162_1949+168del
NM_001126131.2:c.1949+162_1949+168del NP_001119603.1:n.1949+162_1949+168del
NM_002693.3:c.1949+162_1949+168del MANE Select NP_002684.1:n.1949+162_1949+168del