Canonical Allele Identifier: CA2194550774

Gene: POLG

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.89325714T= , CM000677.2:g.89325714T=	GRCh38
NC_000015.9:g.89868945T= , CM000677.1:g.89868945T=	GRCh37
NC_000015.8:g.87669949T=	NCBI36
NG_008218.1:g.14082A=
NG_008218.2:g.14082A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000636937.2:c.1713-28A=	ENSP00000516154.1:n.1713-28A=
ENST00000268124.11:c.1713-28A= MANE Select	ENSP00000268124.5:n.1713-28A=
ENST00000530292.3:c.1314-28A=	ENSP00000432885.2:n.1314-28A=
ENST00000635986.2:c.1713-28A=	ENSP00000490653.2:n.1713-28A=
ENST00000636774.1:c.*280-28A=	ENSP00000489799.1:n.*280-28A=
ENST00000637238.1:c.450-28A=	ENSP00000490756.1:n.450-28A=
ENST00000637264.1:c.785-28A=
ENST00000666746.1:c.1290-28A=
ENST00000670281.1:c.33-28A=	ENSP00000499709.1:n.33-28A=
ENST00000672071.1:n.1911-28A=
ENST00000672923.2:n.1816-28A=
ENST00000268124.9:c.1713-28A=	ENSP00000268124.5:n.1713-28A=
ENST00000442287.6:c.1713-28A=	ENSP00000399851.2:n.1713-28A=
ENST00000526314.2:c.95-28A=
ENST00000631044.2:c.*1096-28A=	ENSP00000486730.1:n.*1096-28A=
NM_001126131.1:c.1713-28A=	NP_001119603.1:n.1713-28A=
NM_002693.2:c.1713-28A=	NP_002684.1:n.1713-28A=
NM_001126131.2:c.1713-28A=	NP_001119603.1:n.1713-28A=
NM_002693.3:c.1713-28A= MANE Select	NP_002684.1:n.1713-28A=