Canonical Allele Identifier: CA2194550949

Gene: POLG

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.89321884T= , CM000677.2:g.89321884T=	GRCh38
NC_000015.9:g.89865115T= , CM000677.1:g.89865115T=	GRCh37
NC_000015.8:g.87666119T=	NCBI36
NG_008218.1:g.17912A=
NG_008218.2:g.17912A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000636937.2:c.2481-31A=	ENSP00000516154.1:n.2481-31A=
ENST00000268124.11:c.2481-31A= MANE Select	ENSP00000268124.5:n.2481-31A=
ENST00000530292.3:c.2082-31A=	ENSP00000432885.2:n.2082-31A=
ENST00000635986.2:c.2481-31A=	ENSP00000490653.2:n.2481-31A=
ENST00000636774.1:c.*1048-31A=	ENSP00000489799.1:n.*1048-31A=
ENST00000637238.1:c.1178-31A=	ENSP00000490756.1:n.1178-31A=
ENST00000637264.1:c.1553-31A=
ENST00000666746.1:c.2058-31A=
ENST00000670281.1:c.800+78A=	ENSP00000499709.1:n.800+78A=
ENST00000672071.1:n.2679-31A=
ENST00000672923.2:n.2423-31A=
ENST00000268124.9:c.2481-31A=	ENSP00000268124.5:n.2481-31A=
ENST00000442287.6:c.2481-31A=	ENSP00000399851.2:n.2481-31A=
ENST00000528881.2:c.196-624A=
ENST00000530715.5:c.185+858A=	ENSP00000431395.1:n.185+858A=
ENST00000532584.5:n.599A=
ENST00000631044.2:c.*1905-31A=	ENSP00000486730.1:n.*1905-31A=
NM_001126131.1:c.2481-31A=	NP_001119603.1:n.2481-31A=
NM_002693.2:c.2481-31A=	NP_002684.1:n.2481-31A=
NM_001126131.2:c.2481-31A=	NP_001119603.1:n.2481-31A=
NM_002693.3:c.2481-31A= MANE Select	NP_002684.1:n.2481-31A=