Canonical Allele Identifier: CA2194539768

Gene: POLG

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.89317614C= , CM000677.2:g.89317614C=	GRCh38
NC_000015.9:g.89860845C= , CM000677.1:g.89860845C=	GRCh37
NC_000015.8:g.87661849C=	NCBI36
NG_008218.1:g.22182G=
NG_011736.1:g.78652C= , LRG_500:g.78652C=
NG_008218.2:g.22182G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000636937.2:c.3483-78G=	ENSP00000516154.1:n.3483-78G=
ENST00000268124.11:c.3483-78G= MANE Select	ENSP00000268124.5:n.3483-78G=
ENST00000530292.3:c.3183-78G=	ENSP00000432885.2:n.3183-78G=
ENST00000635986.2:c.*553-78G=	ENSP00000490653.2:n.*553-78G=
ENST00000636774.1:c.*2087-78G=	ENSP00000489799.1:n.*2087-78G=
ENST00000637042.1:n.72-143G=
ENST00000637238.1:c.2391-78G=	ENSP00000490756.1:n.2391-78G=
ENST00000637264.1:c.2555-138G=
ENST00000666746.1:c.3060-78G=
ENST00000672071.1:n.4607G=
ENST00000672695.1:n.1262-78G=
ENST00000672923.2:n.3483-78G=
ENST00000268124.9:c.3483-78G=	ENSP00000268124.5:n.3483-78G=
ENST00000442287.6:c.3483-78G=	ENSP00000399851.2:n.3483-78G=
ENST00000526671.1:n.215G=
ENST00000530292.2:c.666-78G=	ENSP00000432885.1:n.666-78G=
ENST00000631044.2:c.*2907-78G=	ENSP00000486730.1:n.*2907-78G=
NM_001126131.1:c.3483-78G=	NP_001119603.1:n.3483-78G=
NM_002693.2:c.3483-78G=	NP_002684.1:n.3483-78G=
NM_001126131.2:c.3483-78G=	NP_001119603.1:n.3483-78G=
NM_002693.3:c.3483-78G= MANE Select	NP_002684.1:n.3483-78G=