Canonical Allele Identifier: CA2194561832

Gene: POLG

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.89328779A= , CM000677.2:g.89328779A=	GRCh38
NC_000015.9:g.89872010A= , CM000677.1:g.89872010A=	GRCh37
NC_000015.8:g.87673014A=	NCBI36
NG_008218.1:g.11017T=
NG_008218.2:g.11017T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000636937.2:c.1076T=	ENSP00000516154.1:p.Val359=
ENST00000268124.11:c.1076T= MANE Select	ENSP00000268124.5:p.Val359=
ENST00000530292.3:c.677T=	ENSP00000432885.2:p.Val226=
ENST00000635986.2:c.1076T=	ENSP00000490653.2:p.Val359=
ENST00000636774.1:c.1076T=	ENSP00000489799.1:p.Val359=
ENST00000637264.1:c.148T=
ENST00000666746.1:c.733T=
ENST00000672071.1:n.1274T=
ENST00000672923.2:n.73T=
ENST00000268124.9:c.1076T=	ENSP00000268124.5:p.Val359=
ENST00000442287.6:c.1076T=	ENSP00000399851.2:p.Val359=
ENST00000631044.2:c.*459T=	ENSP00000486730.1:n.*459T=
NM_001126131.1:c.1076T=	NP_001119603.1:p.Val359=
NM_002693.2:c.1076T=	NP_002684.1:p.Val359=
NM_001126131.2:c.1076T=	NP_001119603.1:p.Val359=
NM_002693.3:c.1076T= MANE Select	NP_002684.1:p.Val359=