Canonical Allele Identifier: CA2194539281

Gene: POLG

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.89317469C= , CM000677.2:g.89317469C=	GRCh38
NC_000015.9:g.89860700C= , CM000677.1:g.89860700C=	GRCh37
NC_000015.8:g.87661704C=	NCBI36
NG_008218.1:g.22327G=
NG_011736.1:g.78507C= , LRG_500:g.78507C=
NG_008218.2:g.22327G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000636937.2:c.3550G=	ENSP00000516154.1:p.Asp1184=
ENST00000268124.11:c.3550G= MANE Select	ENSP00000268124.5:p.Asp1184=
ENST00000530292.3:c.3250G=	ENSP00000432885.2:n.3250G=
ENST00000635986.2:c.*620G=	ENSP00000490653.2:n.*620G=
ENST00000636774.1:c.*2154G=	ENSP00000489799.1:n.*2154G=
ENST00000637042.1:n.74G=
ENST00000637238.1:c.2458G=	ENSP00000490756.1:n.2458G=
ENST00000637264.1:c.2562G=
ENST00000666746.1:c.3127G=
ENST00000672071.1:n.4752G=
ENST00000672695.1:n.1329G=
ENST00000672923.2:n.3550G=
ENST00000268124.9:c.3550G=	ENSP00000268124.5:p.Asp1184=
ENST00000442287.6:c.3550G=	ENSP00000399851.2:p.Asp1184=
ENST00000526671.1:n.360G=
ENST00000530292.2:c.733G=	ENSP00000432885.1:n.733G=
ENST00000631044.2:c.*2974G=	ENSP00000486730.1:n.*2974G=
NM_001126131.1:c.3550G=	NP_001119603.1:p.Asp1184=
NM_002693.2:c.3550G=	NP_002684.1:p.Asp1184=
NM_001126131.2:c.3550G=	NP_001119603.1:p.Asp1184=
NM_002693.3:c.3550G= MANE Select	NP_002684.1:p.Asp1184=