Canonical Allele Identifier: CA2194557279

Gene: POLG

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.89327006C= , CM000677.2:g.89327006C=	GRCh38
NC_000015.9:g.89870237C= , CM000677.1:g.89870237C=	GRCh37
NC_000015.8:g.87671241C=	NCBI36
NG_008218.1:g.12790G=
NG_008218.2:g.12790G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000636937.2:c.1491G=	ENSP00000516154.1:p.Gln497=
ENST00000268124.11:c.1491G= MANE Select	ENSP00000268124.5:p.Gln497=
ENST00000530292.3:c.1092G=	ENSP00000432885.2:p.Gln364=
ENST00000635986.2:c.1491G=	ENSP00000490653.2:p.Gln497=
ENST00000636774.1:c.*58G=	ENSP00000489799.1:n.*58G=
ENST00000637238.1:c.228G=	ENSP00000490756.1:p.Gln76=
ENST00000637264.1:c.563G=
ENST00000666746.1:c.1068G=
ENST00000672071.1:n.1689G=
ENST00000672923.2:n.1594G=
ENST00000268124.9:c.1491G=	ENSP00000268124.5:p.Gln497=
ENST00000442287.6:c.1491G=	ENSP00000399851.2:p.Gln497=
ENST00000631044.2:c.*874G=	ENSP00000486730.1:n.*874G=
NM_001126131.1:c.1491G=	NP_001119603.1:p.Gln497=
NM_002693.2:c.1491G=	NP_002684.1:p.Gln497=
NM_001126131.2:c.1491G=	NP_001119603.1:p.Gln497=
NM_002693.3:c.1491G= MANE Select	NP_002684.1:p.Gln497=