Canonical Allele Identifier: CA2194541661
Gene: POLG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.89318586C= , CM000677.2:g.89318586C= GRCh38
NC_000015.9:g.89861817C= , CM000677.1:g.89861817C= GRCh37
NC_000015.8:g.87662821C= NCBI36
NG_008218.1:g.21210G=
NG_011736.1:g.79624C= , LRG_500:g.79624C=
NG_008218.2:g.21210G=

Transcript Alleles

HGVS Amino-acid change
ENST00000636937.2:c.3437G= ENSP00000516154.1:p.Arg1146=
ENST00000268124.11:c.3437G= MANE Select ENSP00000268124.5:p.Arg1146=
ENST00000530292.3:c.3038G= ENSP00000432885.2:p.Arg1013=
ENST00000635986.2:c.*507G= ENSP00000490653.2:n.*507G=
ENST00000636774.1:c.*2004G= ENSP00000489799.1:n.*2004G=
ENST00000637238.1:c.2246G= ENSP00000490756.1:n.2246G=
ENST00000637264.1:c.2509G=
ENST00000666746.1:c.3014G=
ENST00000672071.1:n.3635G=
ENST00000672695.1:n.614G=
ENST00000672923.2:n.3437G=
ENST00000268124.9:c.3437G= ENSP00000268124.5:p.Arg1146=
ENST00000442287.6:c.3437G= ENSP00000399851.2:p.Arg1146=
ENST00000530292.2:c.521G= ENSP00000432885.1:p.Arg174=
ENST00000631044.2:c.*2861G= ENSP00000486730.1:n.*2861G=
NM_001126131.1:c.3437G= NP_001119603.1:p.Arg1146=
NM_002693.2:c.3437G= NP_002684.1:p.Arg1146=
NM_001126131.2:c.3437G= NP_001119603.1:p.Arg1146=
NM_002693.3:c.3437G= MANE Select NP_002684.1:p.Arg1146=