Canonical Allele Identifier: CA2194572118

Gene: POLG POLGARF

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.89333327G= , CM000677.2:g.89333327G=	GRCh38
NC_000015.9:g.89876558G= , CM000677.1:g.89876558G=	GRCh37
NC_000015.8:g.87677562G=	NCBI36
NG_008218.1:g.6469C=
NG_008218.2:g.6469C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000636937.2:c.428C= (POLG)	ENSP00000516154.1:p.Ala143=
ENST00000706918.1:c.483C= (POLGARF)	ENSP00000516626.1:p.Gly161=
ENST00000268124.11:c.428C= (POLG) MANE Select	ENSP00000268124.5:p.Ala143=
ENST00000530292.3:c.29C= (POLG)	ENSP00000432885.2:p.Ala10=
ENST00000635986.2:c.428C= (POLG)	ENSP00000490653.2:p.Ala143=
ENST00000636774.1:c.428C= (POLG)	ENSP00000489799.1:p.Ala143=
ENST00000650303.2:c.483C= (POLG)	ENSP00000497242.2:p.Gly161=
ENST00000666746.1:c.85C= (POLG)
ENST00000672071.1:n.626C= (POLG)
ENST00000268124.9:c.428C= (POLG)	ENSP00000268124.5:p.Ala143=
ENST00000442287.6:c.428C= (POLG)	ENSP00000399851.2:p.Ala143=
ENST00000631044.2:c.428C= (POLG)	ENSP00000486730.1:p.Ala143=
NM_001126131.1:c.428C= (POLG)	NP_001119603.1:p.Ala143=
NM_002693.2:c.428C= (POLG)	NP_002684.1:p.Ala143=
NM_001126131.2:c.428C= (POLG)	NP_001119603.1:p.Ala143=
NM_002693.3:c.428C= (POLG) MANE Select	NP_002684.1:p.Ala143=