Canonical Allele Identifier: CA2194554691
Gene: POLG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.89323238_89323242delinsAAAAC , CM000677.2:g.89323238_89323242delinsAAAAC GRCh38
NC_000015.9:g.89866469_89866473delinsAAAAC , CM000677.1:g.89866469_89866473delinsAAAAC GRCh37
NC_000015.8:g.87667473_87667477delinsAAAAC NCBI36
NG_008218.1:g.16554_16558delinsGTTTT
NG_008218.2:g.16554_16558delinsGTTTT

Transcript Alleles

HGVS Amino-acid change
ENST00000636937.2:c.2265+162_2265+166delinsGTTTT ENSP00000516154.1:n.2265+162_2265+166deli...
ENST00000268124.11:c.2265+162_2265+166delinsGTTTT MANE Select ENSP00000268124.5:n.2265+162_2265+166deli...
ENST00000530292.3:c.1866+162_1866+166delinsGTTTT ENSP00000432885.2:n.1866+162_1866+166deli...
ENST00000635986.2:c.2265+162_2265+166delinsGTTTT ENSP00000490653.2:n.2265+162_2265+166deli...
ENST00000636774.1:c.*832+162_*832+166delinsGTTTT ENSP00000489799.1:n.*832+162_*832+166deli...
ENST00000637238.1:c.962+162_962+166delinsGTTTT ENSP00000490756.1:n.962+162_962+166delins...
ENST00000637264.1:c.1337+162_1337+166delinsGTTTT
ENST00000666746.1:c.1842+162_1842+166delinsGTTTT
ENST00000670281.1:c.585+162_585+166delinsGTTTT ENSP00000499709.1:n.585+162_585+166delins...
ENST00000672071.1:n.2463+162_2463+166delinsGTTTT
ENST00000672923.2:n.2368+162_2368+166delinsGTTTT
ENST00000268124.9:c.2265+162_2265+166delinsGTTTT ENSP00000268124.5:n.2265+162_2265+166deli...
ENST00000442287.6:c.2265+162_2265+166delinsGTTTT ENSP00000399851.2:n.2265+162_2265+166deli...
ENST00000526314.2:c.540-340_540-336delinsGTTTT
ENST00000526398.1:c.414+162_414+166delinsGTTTT
ENST00000528881.2:c.34+162_34+166delinsGTTTT
ENST00000530715.5:c.24+162_24+166delinsGTTTT ENSP00000431395.1:n.24+162_24+166delinsGT...
ENST00000532584.5:n.467+162_467+166delinsGTTTT
ENST00000631044.2:c.*1689+162_*1689+166delinsGTTTT ENSP00000486730.1:n.*1689+162_*1689+166de...
NM_001126131.1:c.2265+162_2265+166delinsGTTTT NP_001119603.1:n.2265+162_2265+166delinsG...
NM_002693.2:c.2265+162_2265+166delinsGTTTT NP_002684.1:n.2265+162_2265+166delinsGTTT...
NM_001126131.2:c.2265+162_2265+166delinsGTTTT NP_001119603.1:n.2265+162_2265+166delinsG...
NM_002693.3:c.2265+162_2265+166delinsGTTTT MANE Select NP_002684.1:n.2265+162_2265+166delinsGTTT...