Canonical Allele Identifier: CA2805168117

Gene: POLG

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.89328876_89328877insAGA , CM000677.2:g.89328876_89328877insAGA	GRCh38
NC_000015.9:g.89872107_89872108insAGA , CM000677.1:g.89872107_89872108insAGA	GRCh37
NC_000015.8:g.87673111_87673112insAGA	NCBI36
NG_008218.1:g.10919_10920insTCT
NG_008218.2:g.10919_10920insTCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000636937.2:c.1024-46_1024-45insTCT	ENSP00000516154.1:n.1024-46_1024-45insTCT
ENST00000268124.11:c.1024-46_1024-45insTCT MANE Select	ENSP00000268124.5:n.1024-46_1024-45insTCT
ENST00000530292.3:c.625-46_625-45insTCT	ENSP00000432885.2:n.625-46_625-45insTCT
ENST00000635986.2:c.1024-46_1024-45insTCT	ENSP00000490653.2:n.1024-46_1024-45insTCT
ENST00000636774.1:c.1024-46_1024-45insTCT	ENSP00000489799.1:n.1024-46_1024-45insTCT
ENST00000637264.1:c.96-46_96-45insTCT
ENST00000666746.1:c.681-46_681-45insTCT
ENST00000672071.1:n.1222-46_1222-45insTCT
ENST00000672923.2:n.21-46_21-45insTCT
ENST00000268124.9:c.1024-46_1024-45insTCT	ENSP00000268124.5:n.1024-46_1024-45insTCT
ENST00000442287.6:c.1024-46_1024-45insTCT	ENSP00000399851.2:n.1024-46_1024-45insTCT
ENST00000631044.2:c.*407-46_*407-45insTCT	ENSP00000486730.1:n.*407-46_*407-45insTCT
NM_001126131.1:c.1024-46_1024-45insTCT	NP_001119603.1:n.1024-46_1024-45insTCT
NM_002693.2:c.1024-46_1024-45insTCT	NP_002684.1:n.1024-46_1024-45insTCT
NM_001126131.2:c.1024-46_1024-45insTCT	NP_001119603.1:n.1024-46_1024-45insTCT
NM_002693.3:c.1024-46_1024-45insTCT MANE Select	NP_002684.1:n.1024-46_1024-45insTCT