Canonical Allele Identifier: CA2194541668
Gene: POLG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.89318587G= , CM000677.2:g.89318587G= GRCh38
NC_000015.9:g.89861818G= , CM000677.1:g.89861818G= GRCh37
NC_000015.8:g.87662822G= NCBI36
NG_008218.1:g.21209C=
NG_011736.1:g.79625G= , LRG_500:g.79625G=
NG_008218.2:g.21209C=

Transcript Alleles

HGVS Amino-acid change
ENST00000636937.2:c.3436C= ENSP00000516154.1:p.Arg1146=
ENST00000268124.11:c.3436C= MANE Select ENSP00000268124.5:p.Arg1146=
ENST00000530292.3:c.3037C= ENSP00000432885.2:p.Arg1013=
ENST00000635986.2:c.*506C= ENSP00000490653.2:n.*506C=
ENST00000636774.1:c.*2003C= ENSP00000489799.1:n.*2003C=
ENST00000637238.1:c.2245C= ENSP00000490756.1:n.2245C=
ENST00000637264.1:c.2508C=
ENST00000666746.1:c.3013C=
ENST00000672071.1:n.3634C=
ENST00000672695.1:n.613C=
ENST00000672923.2:n.3436C=
ENST00000268124.9:c.3436C= ENSP00000268124.5:p.Arg1146=
ENST00000442287.6:c.3436C= ENSP00000399851.2:p.Arg1146=
ENST00000530292.2:c.520C= ENSP00000432885.1:p.Arg174=
ENST00000631044.2:c.*2860C= ENSP00000486730.1:n.*2860C=
NM_001126131.1:c.3436C= NP_001119603.1:p.Arg1146=
NM_002693.2:c.3436C= NP_002684.1:p.Arg1146=
NM_001126131.2:c.3436C= NP_001119603.1:p.Arg1146=
NM_002693.3:c.3436C= MANE Select NP_002684.1:p.Arg1146=