Canonical Allele Identifier: CA2194550581

Gene: POLG

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.89325656G= , CM000677.2:g.89325656G=	GRCh38
NC_000015.9:g.89868887G= , CM000677.1:g.89868887G=	GRCh37
NC_000015.8:g.87669891G=	NCBI36
NG_008218.1:g.14140C=
NG_008218.2:g.14140C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000636937.2:c.1743C=	ENSP00000516154.1:p.Asp581=
ENST00000268124.11:c.1743C= MANE Select	ENSP00000268124.5:p.Asp581=
ENST00000530292.3:c.1344C=	ENSP00000432885.2:p.Asp448=
ENST00000635986.2:c.1743C=	ENSP00000490653.2:p.Asp581=
ENST00000636774.1:c.*310C=	ENSP00000489799.1:n.*310C=
ENST00000637238.1:c.480C=	ENSP00000490756.1:p.Asp160=
ENST00000637264.1:c.815C=
ENST00000666746.1:c.1320C=
ENST00000670281.1:c.63C=	ENSP00000499709.1:p.Asp21=
ENST00000672071.1:n.1941C=
ENST00000672923.2:n.1846C=
ENST00000268124.9:c.1743C=	ENSP00000268124.5:p.Asp581=
ENST00000442287.6:c.1743C=	ENSP00000399851.2:p.Asp581=
ENST00000526314.2:c.125C=
ENST00000631044.2:c.*1126C=	ENSP00000486730.1:n.*1126C=
NM_001126131.1:c.1743C=	NP_001119603.1:p.Asp581=
NM_002693.2:c.1743C=	NP_002684.1:p.Asp581=
NM_001126131.2:c.1743C=	NP_001119603.1:p.Asp581=
NM_002693.3:c.1743C= MANE Select	NP_002684.1:p.Asp581=