Canonical Allele Identifier: CA2194542934
Gene: POLG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.89318984C= , CM000677.2:g.89318984C= GRCh38
NC_000015.9:g.89862215C= , CM000677.1:g.89862215C= GRCh37
NC_000015.8:g.87663219C= NCBI36
NG_008218.1:g.20812G=
NG_011736.1:g.80022C= , LRG_500:g.80022C=
NG_008218.2:g.20812G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000636937.2:c.3220G= ENSP00000516154.1:p.Val1074=
ENST00000268124.11:c.3220G= MANE Select ENSP00000268124.5:p.Val1074=
ENST00000530292.3:c.2821G= ENSP00000432885.2:p.Val941=
ENST00000635986.2:c.*290G= ENSP00000490653.2:n.*290G=
ENST00000636774.1:c.*1787G= ENSP00000489799.1:n.*1787G=
ENST00000637238.1:c.2029G= ENSP00000490756.1:n.2029G=
ENST00000637264.1:c.2292G=
ENST00000666746.1:c.2797G=
ENST00000672071.1:n.3418G=
ENST00000672695.1:n.397G=
ENST00000672923.2:n.3220G=
ENST00000268124.9:c.3220G= ENSP00000268124.5:p.Val1074=
ENST00000442287.6:c.3220G= ENSP00000399851.2:p.Val1074=
ENST00000530292.2:c.304G= ENSP00000432885.1:p.Val102=
ENST00000631044.2:c.*2644G= ENSP00000486730.1:n.*2644G=
NM_001126131.1:c.3220G= NP_001119603.1:p.Val1074=
NM_002693.2:c.3220G= NP_002684.1:p.Val1074=
NM_001126131.2:c.3220G= NP_001119603.1:p.Val1074=
NM_002693.3:c.3220G= MANE Select NP_002684.1:p.Val1074=