Canonical Allele Identifier: CA2194548529
Gene: POLG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.89321112G= , CM000677.2:g.89321112G= GRCh38
NC_000015.9:g.89864343G= , CM000677.1:g.89864343G= GRCh37
NC_000015.8:g.87665347G= NCBI36
NG_008218.1:g.18684C=
NG_008218.2:g.18684C=

Transcript Alleles

HGVS Amino-acid change
ENST00000636937.2:c.2734+13C= ENSP00000516154.1:n.2734+13C=
ENST00000268124.11:c.2734+13C= MANE Select ENSP00000268124.5:n.2734+13C=
ENST00000530292.3:c.2335+13C= ENSP00000432885.2:n.2335+13C=
ENST00000635986.2:c.2734+13C= ENSP00000490653.2:n.2734+13C=
ENST00000636774.1:c.*1301+13C= ENSP00000489799.1:n.*1301+13C=
ENST00000637238.1:c.1444C= ENSP00000490756.1:n.1444C=
ENST00000637264.1:c.1806+13C=
ENST00000666746.1:c.2311+13C=
ENST00000670281.1:c.800+850C= ENSP00000499709.1:n.800+850C=
ENST00000672071.1:n.2932+13C=
ENST00000672923.2:n.2676+13C=
ENST00000268124.9:c.2734+13C= ENSP00000268124.5:n.2734+13C=
ENST00000442287.6:c.2734+13C= ENSP00000399851.2:n.2734+13C=
ENST00000528881.2:c.331+13C=
ENST00000530715.5:c.186-243C= ENSP00000431395.1:n.186-243C=
ENST00000631044.2:c.*2158+13C= ENSP00000486730.1:n.*2158+13C=
NM_001126131.1:c.2734+13C= NP_001119603.1:n.2734+13C=
NM_002693.2:c.2734+13C= NP_002684.1:n.2734+13C=
NM_001126131.2:c.2734+13C= NP_001119603.1:n.2734+13C=
NM_002693.3:c.2734+13C= MANE Select NP_002684.1:n.2734+13C=