Canonical Allele Identifier: CA2194542920
Gene: POLG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.89318978C= , CM000677.2:g.89318978C= GRCh38
NC_000015.9:g.89862209C= , CM000677.1:g.89862209C= GRCh37
NC_000015.8:g.87663213C= NCBI36
NG_008218.1:g.20818G=
NG_011736.1:g.80016C= , LRG_500:g.80016C=
NG_008218.2:g.20818G=

Transcript Alleles

HGVS Amino-acid change
ENST00000636937.2:c.3226G= ENSP00000516154.1:p.Gly1076=
ENST00000268124.11:c.3226G= MANE Select ENSP00000268124.5:p.Gly1076=
ENST00000530292.3:c.2827G= ENSP00000432885.2:p.Gly943=
ENST00000635986.2:c.*296G= ENSP00000490653.2:n.*296G=
ENST00000636774.1:c.*1793G= ENSP00000489799.1:n.*1793G=
ENST00000637238.1:c.2035G= ENSP00000490756.1:n.2035G=
ENST00000637264.1:c.2298G=
ENST00000666746.1:c.2803G=
ENST00000672071.1:n.3424G=
ENST00000672695.1:n.403G=
ENST00000672923.2:n.3226G=
ENST00000268124.9:c.3226G= ENSP00000268124.5:p.Gly1076=
ENST00000442287.6:c.3226G= ENSP00000399851.2:p.Gly1076=
ENST00000530292.2:c.310G= ENSP00000432885.1:p.Gly104=
ENST00000631044.2:c.*2650G= ENSP00000486730.1:n.*2650G=
NM_001126131.1:c.3226G= NP_001119603.1:p.Gly1076=
NM_002693.2:c.3226G= NP_002684.1:p.Gly1076=
NM_001126131.2:c.3226G= NP_001119603.1:p.Gly1076=
NM_002693.3:c.3226G= MANE Select NP_002684.1:p.Gly1076=