Canonical Allele Identifier: CA2194555654

Gene: POLG

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.89323510G= , CM000677.2:g.89323510G=	GRCh38
NC_000015.9:g.89866741G= , CM000677.1:g.89866741G=	GRCh37
NC_000015.8:g.87667745G=	NCBI36
NG_008218.1:g.16286C=
NG_008218.2:g.16286C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000636937.2:c.2159C=	ENSP00000516154.1:p.Thr720=
ENST00000268124.11:c.2159C= MANE Select	ENSP00000268124.5:p.Thr720=
ENST00000530292.3:c.1760C=	ENSP00000432885.2:p.Thr587=
ENST00000635986.2:c.2159C=	ENSP00000490653.2:p.Thr720=
ENST00000636774.1:c.*726C=	ENSP00000489799.1:n.*726C=
ENST00000637238.1:c.856C=	ENSP00000490756.1:n.856C=
ENST00000637264.1:c.1231C=
ENST00000666746.1:c.1736C=
ENST00000670281.1:c.479C=	ENSP00000499709.1:p.Thr160=
ENST00000672071.1:n.2357C=
ENST00000672923.2:n.2262C=
ENST00000268124.9:c.2159C=	ENSP00000268124.5:p.Thr720=
ENST00000442287.6:c.2159C=	ENSP00000399851.2:p.Thr720=
ENST00000526314.2:c.539+305C=
ENST00000526398.1:c.308C=
ENST00000532584.5:n.361C=
ENST00000631044.2:c.*1583C=	ENSP00000486730.1:n.*1583C=
NM_001126131.1:c.2159C=	NP_001119603.1:p.Thr720=
NM_002693.2:c.2159C=	NP_002684.1:p.Thr720=
NM_001126131.2:c.2159C=	NP_001119603.1:p.Thr720=
NM_002693.3:c.2159C= MANE Select	NP_002684.1:p.Thr720=