Canonical Allele Identifier: CA2194550439

Gene: POLG

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.89321759A= , CM000677.2:g.89321759A=	GRCh38
NC_000015.9:g.89864990A= , CM000677.1:g.89864990A=	GRCh37
NC_000015.8:g.87665994A=	NCBI36
NG_008218.1:g.18037T=
NG_008218.2:g.18037T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000636937.2:c.2575T=	ENSP00000516154.1:p.Trp859=
ENST00000268124.11:c.2575T= MANE Select	ENSP00000268124.5:p.Trp859=
ENST00000530292.3:c.2176T=	ENSP00000432885.2:p.Trp726=
ENST00000635986.2:c.2575T=	ENSP00000490653.2:p.Trp859=
ENST00000636774.1:c.*1142T=	ENSP00000489799.1:n.*1142T=
ENST00000637238.1:c.1272T=	ENSP00000490756.1:n.1272T=
ENST00000637264.1:c.1647T=
ENST00000666746.1:c.2152T=
ENST00000670281.1:c.800+203T=	ENSP00000499709.1:n.800+203T=
ENST00000672071.1:n.2773T=
ENST00000672923.2:n.2517T=
ENST00000268124.9:c.2575T=	ENSP00000268124.5:p.Trp859=
ENST00000442287.6:c.2575T=	ENSP00000399851.2:p.Trp859=
ENST00000528881.2:c.196-499T=
ENST00000530715.5:c.186-890T=	ENSP00000431395.1:n.186-890T=
ENST00000631044.2:c.*1999T=	ENSP00000486730.1:n.*1999T=
NM_001126131.1:c.2575T=	NP_001119603.1:p.Trp859=
NM_002693.2:c.2575T=	NP_002684.1:p.Trp859=
NM_001126131.2:c.2575T=	NP_001119603.1:p.Trp859=
NM_002693.3:c.2575T= MANE Select	NP_002684.1:p.Trp859=