Canonical Allele Identifier: CA2194561977

Gene: POLG

Linked Data

• dbSNP Id: rs2055557186

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.89328835_89328836insA , CM000677.2:g.89328835_89328836insA	GRCh38
NC_000015.9:g.89872066_89872067insA , CM000677.1:g.89872066_89872067insA	GRCh37
NC_000015.8:g.87673070_87673071insA	NCBI36
NG_008218.1:g.10960_10961insT
NG_008218.2:g.10960_10961insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000636937.2:c.1024-5_1024-4insT	ENSP00000516154.1:n.1024-5_1024-4insT
ENST00000268124.11:c.1024-5_1024-4insT MANE Select	ENSP00000268124.5:n.1024-5_1024-4insT
ENST00000530292.3:c.625-5_625-4insT	ENSP00000432885.2:n.625-5_625-4insT
ENST00000635986.2:c.1024-5_1024-4insT	ENSP00000490653.2:n.1024-5_1024-4insT
ENST00000636774.1:c.1024-5_1024-4insT	ENSP00000489799.1:n.1024-5_1024-4insT
ENST00000637264.1:c.96-5_96-4insT
ENST00000666746.1:c.681-5_681-4insT
ENST00000672071.1:n.1222-5_1222-4insT
ENST00000672923.2:n.21-5_21-4insT
ENST00000268124.9:c.1024-5_1024-4insT	ENSP00000268124.5:n.1024-5_1024-4insT
ENST00000442287.6:c.1024-5_1024-4insT	ENSP00000399851.2:n.1024-5_1024-4insT
ENST00000631044.2:c.*407-5_*407-4insT	ENSP00000486730.1:n.*407-5_*407-4insT
NM_001126131.1:c.1024-5_1024-4insT	NP_001119603.1:n.1024-5_1024-4insT
NM_002693.2:c.1024-5_1024-4insT	NP_002684.1:n.1024-5_1024-4insT
NM_001126131.2:c.1024-5_1024-4insT	NP_001119603.1:n.1024-5_1024-4insT
NM_002693.3:c.1024-5_1024-4insT MANE Select	NP_002684.1:n.1024-5_1024-4insT