Canonical Allele Identifier: CA2194564452

Gene: POLG

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.89329782_89329783delinsAG , CM000677.2:g.89329782_89329783delinsAG	GRCh38
NC_000015.9:g.89873013_89873014delinsAG , CM000677.1:g.89873013_89873014delinsAG	GRCh37
NC_000015.8:g.87674017_87674018delinsAG	NCBI36
NG_008218.1:g.10013_10014delinsCT
NG_008218.2:g.10013_10014delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000636937.2:c.855+298_855+299delinsCT	ENSP00000516154.1:n.855+298_855+299delinsCT
ENST00000268124.11:c.855+298_855+299delinsCT MANE Select	ENSP00000268124.5:n.855+298_855+299delinsCT
ENST00000530292.3:c.456+298_456+299delinsCT	ENSP00000432885.2:n.456+298_456+299delinsCT
ENST00000635986.2:c.855+298_855+299delinsCT	ENSP00000490653.2:n.855+298_855+299delinsCT
ENST00000636774.1:c.855+298_855+299delinsCT	ENSP00000489799.1:n.855+298_855+299delinsCT
ENST00000666746.1:c.512+298_512+299delinsCT
ENST00000672071.1:n.1053+298_1053+299delinsCT
ENST00000268124.9:c.855+298_855+299delinsCT	ENSP00000268124.5:n.855+298_855+299delinsCT
ENST00000442287.6:c.855+298_855+299delinsCT	ENSP00000399851.2:n.855+298_855+299delinsCT
ENST00000631044.2:c.*238+298_*238+299delinsCT	ENSP00000486730.1:n.*238+298_*238+299delinsCT
NM_001126131.1:c.855+298_855+299delinsCT	NP_001119603.1:n.855+298_855+299delinsCT
NM_002693.2:c.855+298_855+299delinsCT	NP_002684.1:n.855+298_855+299delinsCT
NM_001126131.2:c.855+298_855+299delinsCT	NP_001119603.1:n.855+298_855+299delinsCT
NM_002693.3:c.855+298_855+299delinsCT MANE Select	NP_002684.1:n.855+298_855+299delinsCT