Canonical Allele Identifier: CA2194554988
Gene: POLG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.89323348T= , CM000677.2:g.89323348T= GRCh38
NC_000015.9:g.89866579T= , CM000677.1:g.89866579T= GRCh37
NC_000015.8:g.87667583T= NCBI36
NG_008218.1:g.16448A=
NG_008218.2:g.16448A=

Transcript Alleles

HGVS Amino-acid change
ENST00000636937.2:c.2265+56A= ENSP00000516154.1:n.2265+56A=
ENST00000268124.11:c.2265+56A= MANE Select ENSP00000268124.5:n.2265+56A=
ENST00000530292.3:c.1866+56A= ENSP00000432885.2:n.1866+56A=
ENST00000635986.2:c.2265+56A= ENSP00000490653.2:n.2265+56A=
ENST00000636774.1:c.*832+56A= ENSP00000489799.1:n.*832+56A=
ENST00000637238.1:c.962+56A= ENSP00000490756.1:n.962+56A=
ENST00000637264.1:c.1337+56A=
ENST00000666746.1:c.1842+56A=
ENST00000670281.1:c.585+56A= ENSP00000499709.1:n.585+56A=
ENST00000672071.1:n.2463+56A=
ENST00000672923.2:n.2368+56A=
ENST00000268124.9:c.2265+56A= ENSP00000268124.5:n.2265+56A=
ENST00000442287.6:c.2265+56A= ENSP00000399851.2:n.2265+56A=
ENST00000526314.2:c.540-446A=
ENST00000526398.1:c.414+56A=
ENST00000528881.2:c.34+56A=
ENST00000530715.5:c.24+56A= ENSP00000431395.1:n.24+56A=
ENST00000532584.5:n.467+56A=
ENST00000631044.2:c.*1689+56A= ENSP00000486730.1:n.*1689+56A=
NM_001126131.1:c.2265+56A= NP_001119603.1:n.2265+56A=
NM_002693.2:c.2265+56A= NP_002684.1:n.2265+56A=
NM_001126131.2:c.2265+56A= NP_001119603.1:n.2265+56A=
NM_002693.3:c.2265+56A= MANE Select NP_002684.1:n.2265+56A=