Canonical Allele Identifier: CA2194550556
Gene: POLG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.89321780G= , CM000677.2:g.89321780G= GRCh38
NC_000015.9:g.89865011G= , CM000677.1:g.89865011G= GRCh37
NC_000015.8:g.87666015G= NCBI36
NG_008218.1:g.18016C=
NG_008218.2:g.18016C=

Transcript Alleles

HGVS Amino-acid change
ENST00000636937.2:c.2554C= ENSP00000516154.1:p.Arg852=
ENST00000268124.11:c.2554C= MANE Select ENSP00000268124.5:p.Arg852=
ENST00000530292.3:c.2155C= ENSP00000432885.2:p.Arg719=
ENST00000635986.2:c.2554C= ENSP00000490653.2:p.Arg852=
ENST00000636774.1:c.*1121C= ENSP00000489799.1:n.*1121C=
ENST00000637238.1:c.1251C= ENSP00000490756.1:n.1251C=
ENST00000637264.1:c.1626C=
ENST00000666746.1:c.2131C=
ENST00000670281.1:c.800+182C= ENSP00000499709.1:n.800+182C=
ENST00000672071.1:n.2752C=
ENST00000672923.2:n.2496C=
ENST00000268124.9:c.2554C= ENSP00000268124.5:p.Arg852=
ENST00000442287.6:c.2554C= ENSP00000399851.2:p.Arg852=
ENST00000528881.2:c.196-520C=
ENST00000530715.5:c.186-911C= ENSP00000431395.1:n.186-911C=
ENST00000532584.5:n.703C=
ENST00000631044.2:c.*1978C= ENSP00000486730.1:n.*1978C=
NM_001126131.1:c.2554C= NP_001119603.1:p.Arg852=
NM_002693.2:c.2554C= NP_002684.1:p.Arg852=
NM_001126131.2:c.2554C= NP_001119603.1:p.Arg852=
NM_002693.3:c.2554C= MANE Select NP_002684.1:p.Arg852=