Canonical Allele Identifier: CA2194543285
Gene: POLG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.89319082C= , CM000677.2:g.89319082C= GRCh38
NC_000015.9:g.89862313C= , CM000677.1:g.89862313C= GRCh37
NC_000015.8:g.87663317C= NCBI36
NG_008218.1:g.20714G=
NG_011736.1:g.80120C= , LRG_500:g.80120C=
NG_008218.2:g.20714G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000636937.2:c.3122G= ENSP00000516154.1:p.Trp1041=
ENST00000268124.11:c.3122G= MANE Select ENSP00000268124.5:p.Trp1041=
ENST00000530292.3:c.2723G= ENSP00000432885.2:p.Trp908=
ENST00000635986.2:c.*192G= ENSP00000490653.2:n.*192G=
ENST00000636530.1:n.82G=
ENST00000636774.1:c.*1689G= ENSP00000489799.1:n.*1689G=
ENST00000637238.1:c.1931G= ENSP00000490756.1:n.1931G=
ENST00000637264.1:c.2194G=
ENST00000666746.1:c.2699G=
ENST00000672071.1:n.3320G=
ENST00000672695.1:n.299G=
ENST00000672923.2:n.3122G=
ENST00000268124.9:c.3122G= ENSP00000268124.5:p.Trp1041=
ENST00000442287.6:c.3122G= ENSP00000399851.2:p.Trp1041=
ENST00000530292.2:c.206G= ENSP00000432885.1:p.Trp69=
ENST00000631044.2:c.*2546G= ENSP00000486730.1:n.*2546G=
NM_001126131.1:c.3122G= NP_001119603.1:p.Trp1041=
NM_002693.2:c.3122G= NP_002684.1:p.Trp1041=
NM_001126131.2:c.3122G= NP_001119603.1:p.Trp1041=
NM_002693.3:c.3122G= MANE Select NP_002684.1:p.Trp1041=