Canonical Allele Identifier: CA2194555717

Gene: POLG

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.89323525A= , CM000677.2:g.89323525A=	GRCh38
NC_000015.9:g.89866756A= , CM000677.1:g.89866756A=	GRCh37
NC_000015.8:g.87667760A=	NCBI36
NG_008218.1:g.16271T=
NG_008218.2:g.16271T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000636937.2:c.2158-14T=	ENSP00000516154.1:n.2158-14T=
ENST00000268124.11:c.2158-14T= MANE Select	ENSP00000268124.5:n.2158-14T=
ENST00000530292.3:c.1759-14T=	ENSP00000432885.2:n.1759-14T=
ENST00000635986.2:c.2158-14T=	ENSP00000490653.2:n.2158-14T=
ENST00000636774.1:c.*725-14T=	ENSP00000489799.1:n.*725-14T=
ENST00000637238.1:c.855-14T=	ENSP00000490756.1:n.855-14T=
ENST00000637264.1:c.1230-14T=
ENST00000666746.1:c.1735-14T=
ENST00000670281.1:c.478-14T=	ENSP00000499709.1:n.478-14T=
ENST00000672071.1:n.2356-14T=
ENST00000672923.2:n.2261-14T=
ENST00000268124.9:c.2158-14T=	ENSP00000268124.5:n.2158-14T=
ENST00000442287.6:c.2158-14T=	ENSP00000399851.2:n.2158-14T=
ENST00000526314.2:c.539+290T=
ENST00000526398.1:c.307-14T=
ENST00000526573.1:n.533T=
ENST00000532584.5:n.360-14T=
ENST00000533857.1:n.562T=
ENST00000631044.2:c.*1568T=	ENSP00000486730.1:n.*1568T=
NM_001126131.1:c.2158-14T=	NP_001119603.1:n.2158-14T=
NM_002693.2:c.2158-14T=	NP_002684.1:n.2158-14T=
NM_001126131.2:c.2158-14T=	NP_001119603.1:n.2158-14T=
NM_002693.3:c.2158-14T= MANE Select	NP_002684.1:n.2158-14T=