Canonical Allele Identifier: CA2194550852

Gene: POLG

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.89321859G= , CM000677.2:g.89321859G=	GRCh38
NC_000015.9:g.89865090G= , CM000677.1:g.89865090G=	GRCh37
NC_000015.8:g.87666094G=	NCBI36
NG_008218.1:g.17937C=
NG_008218.2:g.17937C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000636937.2:c.2481-6C=	ENSP00000516154.1:n.2481-6C=
ENST00000268124.11:c.2481-6C= MANE Select	ENSP00000268124.5:n.2481-6C=
ENST00000530292.3:c.2082-6C=	ENSP00000432885.2:n.2082-6C=
ENST00000635986.2:c.2481-6C=	ENSP00000490653.2:n.2481-6C=
ENST00000636774.1:c.*1048-6C=	ENSP00000489799.1:n.*1048-6C=
ENST00000637238.1:c.1178-6C=	ENSP00000490756.1:n.1178-6C=
ENST00000637264.1:c.1553-6C=
ENST00000666746.1:c.2058-6C=
ENST00000670281.1:c.800+103C=	ENSP00000499709.1:n.800+103C=
ENST00000672071.1:n.2679-6C=
ENST00000672923.2:n.2423-6C=
ENST00000268124.9:c.2481-6C=	ENSP00000268124.5:n.2481-6C=
ENST00000442287.6:c.2481-6C=	ENSP00000399851.2:n.2481-6C=
ENST00000528881.2:c.196-599C=
ENST00000530715.5:c.185+883C=	ENSP00000431395.1:n.185+883C=
ENST00000532584.5:n.624C=
ENST00000631044.2:c.*1905-6C=	ENSP00000486730.1:n.*1905-6C=
NM_001126131.1:c.2481-6C=	NP_001119603.1:n.2481-6C=
NM_002693.2:c.2481-6C=	NP_002684.1:n.2481-6C=
NM_001126131.2:c.2481-6C=	NP_001119603.1:n.2481-6C=
NM_002693.3:c.2481-6C= MANE Select	NP_002684.1:n.2481-6C=