Canonical Allele Identifier: CA2194551039

Gene: POLG

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.89325761A= , CM000677.2:g.89325761A=	GRCh38
NC_000015.9:g.89868992A= , CM000677.1:g.89868992A=	GRCh37
NC_000015.8:g.87669996A=	NCBI36
NG_008218.1:g.14035T=
NG_008218.2:g.14035T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000636937.2:c.1713-75T=	ENSP00000516154.1:n.1713-75T=
ENST00000268124.11:c.1713-75T= MANE Select	ENSP00000268124.5:n.1713-75T=
ENST00000530292.3:c.1314-75T=	ENSP00000432885.2:n.1314-75T=
ENST00000635986.2:c.1713-75T=	ENSP00000490653.2:n.1713-75T=
ENST00000636774.1:c.*280-75T=	ENSP00000489799.1:n.*280-75T=
ENST00000637238.1:c.450-75T=	ENSP00000490756.1:n.450-75T=
ENST00000637264.1:c.785-75T=
ENST00000666746.1:c.1290-75T=
ENST00000670281.1:c.33-75T=	ENSP00000499709.1:n.33-75T=
ENST00000672071.1:n.1911-75T=
ENST00000672923.2:n.1816-75T=
ENST00000268124.9:c.1713-75T=	ENSP00000268124.5:n.1713-75T=
ENST00000442287.6:c.1713-75T=	ENSP00000399851.2:n.1713-75T=
ENST00000526314.2:c.95-75T=
ENST00000631044.2:c.*1096-75T=	ENSP00000486730.1:n.*1096-75T=
NM_001126131.1:c.1713-75T=	NP_001119603.1:n.1713-75T=
NM_002693.2:c.1713-75T=	NP_002684.1:n.1713-75T=
NM_001126131.2:c.1713-75T=	NP_001119603.1:n.1713-75T=
NM_002693.3:c.1713-75T= MANE Select	NP_002684.1:n.1713-75T=