Canonical Allele Identifier: CA2805168271

Gene: POLG POLGARF

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.89330453_89330454insACA , CM000677.2:g.89330453_89330454insACA	GRCh38
NC_000015.9:g.89873684_89873685insACA , CM000677.1:g.89873684_89873685insACA	GRCh37
NC_000015.8:g.87674688_87674689insACA	NCBI36
NG_008218.1:g.9342_9343insTGT
NG_008218.2:g.9342_9343insTGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000636937.2:c.660-178_660-177insTGT (POLG)	ENSP00000516154.1:n.660-178_660-177insTGT
ENST00000706918.1:c.715-178_715-177insTGT (POLGARF)	ENSP00000516626.1:n.715-178_715-177insTGT
ENST00000268124.11:c.660-178_660-177insTGT (POLG) MANE Select	ENSP00000268124.5:n.660-178_660-177insTGT
ENST00000530292.3:c.261-178_261-177insTGT (POLG)	ENSP00000432885.2:n.261-178_261-177insTGT
ENST00000635986.2:c.660-178_660-177insTGT (POLG)	ENSP00000490653.2:n.660-178_660-177insTGT
ENST00000636774.1:c.660-178_660-177insTGT (POLG)	ENSP00000489799.1:n.660-178_660-177insTGT
ENST00000637307.1:c.50-193_50-192insTGT (POLG)
ENST00000650303.2:c.715-178_715-177insTGT (POLG)	ENSP00000497242.2:n.715-178_715-177insTGT
ENST00000666746.1:c.317-178_317-177insTGT (POLG)
ENST00000672071.1:n.858-178_858-177insTGT (POLG)
ENST00000268124.9:c.660-178_660-177insTGT (POLG)	ENSP00000268124.5:n.660-178_660-177insTGT
ENST00000442287.6:c.660-178_660-177insTGT (POLG)	ENSP00000399851.2:n.660-178_660-177insTGT
ENST00000631044.2:c.*43-178_*43-177insTGT (POLG)	ENSP00000486730.1:n.*43-178_*43-177insTGT
NM_001126131.1:c.660-178_660-177insTGT (POLG)	NP_001119603.1:n.660-178_660-177insTGT
NM_002693.2:c.660-178_660-177insTGT (POLG)	NP_002684.1:n.660-178_660-177insTGT
NM_001126131.2:c.660-178_660-177insTGT (POLG)	NP_001119603.1:n.660-178_660-177insTGT
NM_002693.3:c.660-178_660-177insTGT (POLG) MANE Select	NP_002684.1:n.660-178_660-177insTGT