Canonical Allele Identifier: CA2194565879

Gene: POLG POLGARF

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.89330305A= , CM000677.2:g.89330305A=	GRCh38
NC_000015.9:g.89873536A= , CM000677.1:g.89873536A=	GRCh37
NC_000015.8:g.87674540A=	NCBI36
NG_008218.1:g.9491T=
NG_008218.2:g.9491T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000636937.2:c.660-29T= (POLG)	ENSP00000516154.1:n.660-29T=
ENST00000706918.1:c.715-29T= (POLGARF)	ENSP00000516626.1:n.715-29T=
ENST00000268124.11:c.660-29T= (POLG) MANE Select	ENSP00000268124.5:n.660-29T=
ENST00000530292.3:c.261-29T= (POLG)	ENSP00000432885.2:n.261-29T=
ENST00000635986.2:c.660-29T= (POLG)	ENSP00000490653.2:n.660-29T=
ENST00000636774.1:c.660-29T= (POLG)	ENSP00000489799.1:n.660-29T=
ENST00000637307.1:c.50-44T= (POLG)
ENST00000650303.2:c.715-29T= (POLG)	ENSP00000497242.2:n.715-29T=
ENST00000666746.1:c.317-29T= (POLG)
ENST00000672071.1:n.858-29T= (POLG)
ENST00000268124.9:c.660-29T= (POLG)	ENSP00000268124.5:n.660-29T=
ENST00000442287.6:c.660-29T= (POLG)	ENSP00000399851.2:n.660-29T=
ENST00000631044.2:c.*43-29T= (POLG)	ENSP00000486730.1:n.*43-29T=
NM_001126131.1:c.660-29T= (POLG)	NP_001119603.1:n.660-29T=
NM_002693.2:c.660-29T= (POLG)	NP_002684.1:n.660-29T=
NM_001126131.2:c.660-29T= (POLG)	NP_001119603.1:n.660-29T=
NM_002693.3:c.660-29T= (POLG) MANE Select	NP_002684.1:n.660-29T=