Canonical Allele Identifier: CA2194558448

Gene: POLG

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.89327345G= , CM000677.2:g.89327345G=	GRCh38
NC_000015.9:g.89870576G= , CM000677.1:g.89870576G=	GRCh37
NC_000015.8:g.87671580G=	NCBI36
NG_008218.1:g.12451C=
NG_008218.2:g.12451C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000636937.2:c.1255C=	ENSP00000516154.1:p.Pro419=
ENST00000268124.11:c.1255C= MANE Select	ENSP00000268124.5:p.Pro419=
ENST00000530292.3:c.856C=	ENSP00000432885.2:p.Pro286=
ENST00000635986.2:c.1255C=	ENSP00000490653.2:p.Pro419=
ENST00000636774.1:c.1255C=	ENSP00000489799.1:p.Pro419=
ENST00000637264.1:c.327C=
ENST00000666746.1:c.832C=
ENST00000672071.1:n.1453C=
ENST00000672923.2:n.1358C=
ENST00000268124.9:c.1255C=	ENSP00000268124.5:p.Pro419=
ENST00000442287.6:c.1255C=	ENSP00000399851.2:p.Pro419=
ENST00000532363.2:n.113C=
ENST00000631044.2:c.*638C=	ENSP00000486730.1:n.*638C=
NM_001126131.1:c.1255C=	NP_001119603.1:p.Pro419=
NM_002693.2:c.1255C=	NP_002684.1:p.Pro419=
NM_001126131.2:c.1255C=	NP_001119603.1:p.Pro419=
NM_002693.3:c.1255C= MANE Select	NP_002684.1:p.Pro419=