Canonical Allele Identifier: CA2194555397
Gene: POLG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.89323452G= , CM000677.2:g.89323452G= GRCh38
NC_000015.9:g.89866683G= , CM000677.1:g.89866683G= GRCh37
NC_000015.8:g.87667687G= NCBI36
NG_008218.1:g.16344C=
NG_008218.2:g.16344C=

Transcript Alleles

HGVS Amino-acid change
ENST00000636937.2:c.2217C= ENSP00000516154.1:p.Tyr739=
ENST00000268124.11:c.2217C= MANE Select ENSP00000268124.5:p.Tyr739=
ENST00000530292.3:c.1818C= ENSP00000432885.2:p.Tyr606=
ENST00000635986.2:c.2217C= ENSP00000490653.2:p.Tyr739=
ENST00000636774.1:c.*784C= ENSP00000489799.1:n.*784C=
ENST00000637238.1:c.914C= ENSP00000490756.1:n.914C=
ENST00000637264.1:c.1289C=
ENST00000666746.1:c.1794C=
ENST00000670281.1:c.537C= ENSP00000499709.1:p.Tyr179=
ENST00000672071.1:n.2415C=
ENST00000672923.2:n.2320C=
ENST00000268124.9:c.2217C= ENSP00000268124.5:p.Tyr739=
ENST00000442287.6:c.2217C= ENSP00000399851.2:p.Tyr739=
ENST00000526314.2:c.539+363C=
ENST00000526398.1:c.366C=
ENST00000532584.5:n.419C=
ENST00000631044.2:c.*1641C= ENSP00000486730.1:n.*1641C=
NM_001126131.1:c.2217C= NP_001119603.1:p.Tyr739=
NM_002693.2:c.2217C= NP_002684.1:p.Tyr739=
NM_001126131.2:c.2217C= NP_001119603.1:p.Tyr739=
NM_002693.3:c.2217C= MANE Select NP_002684.1:p.Tyr739=