Canonical Allele Identifier: CA2194563009
Gene: POLG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.89329116G= , CM000677.2:g.89329116G= GRCh38
NC_000015.9:g.89872347G= , CM000677.1:g.89872347G= GRCh37
NC_000015.8:g.87673351G= NCBI36
NG_008218.1:g.10680C=
NG_008218.2:g.10680C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000636937.2:c.856-6C= ENSP00000516154.1:n.856-6C=
ENST00000268124.11:c.856-6C= MANE Select ENSP00000268124.5:n.856-6C=
ENST00000530292.3:c.457-6C= ENSP00000432885.2:n.457-6C=
ENST00000635986.2:c.856-6C= ENSP00000490653.2:n.856-6C=
ENST00000636774.1:c.856-6C= ENSP00000489799.1:n.856-6C=
ENST00000666746.1:c.513-6C=
ENST00000672071.1:n.1054-6C=
ENST00000268124.9:c.856-6C= ENSP00000268124.5:n.856-6C=
ENST00000442287.6:c.856-6C= ENSP00000399851.2:n.856-6C=
ENST00000631044.2:c.*239-6C= ENSP00000486730.1:n.*239-6C=
NM_001126131.1:c.856-6C= NP_001119603.1:n.856-6C=
NM_002693.2:c.856-6C= NP_002684.1:n.856-6C=
NM_001126131.2:c.856-6C= NP_001119603.1:n.856-6C=
NM_002693.3:c.856-6C= MANE Select NP_002684.1:n.856-6C=