Canonical Allele Identifier: CA2194541606
Gene: POLG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.89318578C= , CM000677.2:g.89318578C= GRCh38
NC_000015.9:g.89861809C= , CM000677.1:g.89861809C= GRCh37
NC_000015.8:g.87662813C= NCBI36
NG_008218.1:g.21218G=
NG_011736.1:g.79616C= , LRG_500:g.79616C=
NG_008218.2:g.21218G=

Transcript Alleles

HGVS Amino-acid change
ENST00000636937.2:c.3445G= ENSP00000516154.1:p.Ala1149=
ENST00000268124.11:c.3445G= MANE Select ENSP00000268124.5:p.Ala1149=
ENST00000530292.3:c.3046G= ENSP00000432885.2:p.Ala1016=
ENST00000635986.2:c.*515G= ENSP00000490653.2:n.*515G=
ENST00000636774.1:c.*2012G= ENSP00000489799.1:n.*2012G=
ENST00000637238.1:c.2254G= ENSP00000490756.1:n.2254G=
ENST00000637264.1:c.2517G=
ENST00000666746.1:c.3022G=
ENST00000672071.1:n.3643G=
ENST00000672695.1:n.622G=
ENST00000672923.2:n.3445G=
ENST00000268124.9:c.3445G= ENSP00000268124.5:p.Ala1149=
ENST00000442287.6:c.3445G= ENSP00000399851.2:p.Ala1149=
ENST00000530292.2:c.529G= ENSP00000432885.1:p.Ala177=
ENST00000631044.2:c.*2869G= ENSP00000486730.1:n.*2869G=
NM_001126131.1:c.3445G= NP_001119603.1:p.Ala1149=
NM_002693.2:c.3445G= NP_002684.1:p.Ala1149=
NM_001126131.2:c.3445G= NP_001119603.1:p.Ala1149=
NM_002693.3:c.3445G= MANE Select NP_002684.1:p.Ala1149=