Canonical Allele Identifier: CA2194549828

Gene: POLG

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.89325468C= , CM000677.2:g.89325468C=	GRCh38
NC_000015.9:g.89868699C= , CM000677.1:g.89868699C=	GRCh37
NC_000015.8:g.87669703C=	NCBI36
NG_008218.1:g.14328G=
NG_008218.2:g.14328G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000636937.2:c.1931G=	ENSP00000516154.1:p.Gly644=
ENST00000268124.11:c.1931G= MANE Select	ENSP00000268124.5:p.Gly644=
ENST00000530292.3:c.1532G=	ENSP00000432885.2:p.Gly511=
ENST00000635986.2:c.1931G=	ENSP00000490653.2:p.Gly644=
ENST00000636774.1:c.*498G=	ENSP00000489799.1:n.*498G=
ENST00000637238.1:c.646+22G=	ENSP00000490756.1:n.646+22G=
ENST00000637264.1:c.1003G=
ENST00000666746.1:c.1508G=
ENST00000670281.1:c.251G=	ENSP00000499709.1:p.Gly84=
ENST00000672071.1:n.2129G=
ENST00000672923.2:n.2034G=
ENST00000268124.9:c.1931G=	ENSP00000268124.5:p.Gly644=
ENST00000442287.6:c.1931G=	ENSP00000399851.2:p.Gly644=
ENST00000526314.2:c.313G=
ENST00000526398.1:c.120G=
ENST00000526573.1:n.17G=
ENST00000532584.5:n.133G=
ENST00000631044.2:c.*1314G=	ENSP00000486730.1:n.*1314G=
NM_001126131.1:c.1931G=	NP_001119603.1:p.Gly644=
NM_002693.2:c.1931G=	NP_002684.1:p.Gly644=
NM_001126131.2:c.1931G=	NP_001119603.1:p.Gly644=
NM_002693.3:c.1931G= MANE Select	NP_002684.1:p.Gly644=