Canonical Allele Identifier: CA2194563277

Gene: POLG

Linked Data

• dbSNP Id: rs2055564335

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.89329240_89329241del , CM000677.2:g.89329240_89329241del	GRCh38
NC_000015.9:g.89872471_89872472del , CM000677.1:g.89872471_89872472del	GRCh37
NC_000015.8:g.87673475_87673476del	NCBI36
NG_008218.1:g.10559_10560del
NG_008218.2:g.10559_10560del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000636937.2:c.856-127_856-126del	ENSP00000516154.1:n.856-127_856-126del
ENST00000268124.11:c.856-127_856-126del MANE Select	ENSP00000268124.5:n.856-127_856-126del
ENST00000530292.3:c.457-127_457-126del	ENSP00000432885.2:n.457-127_457-126del
ENST00000635986.2:c.856-127_856-126del	ENSP00000490653.2:n.856-127_856-126del
ENST00000636774.1:c.856-127_856-126del	ENSP00000489799.1:n.856-127_856-126del
ENST00000666746.1:c.513-127_513-126del
ENST00000672071.1:n.1054-127_1054-126del
ENST00000268124.9:c.856-127_856-126del	ENSP00000268124.5:n.856-127_856-126del
ENST00000442287.6:c.856-127_856-126del	ENSP00000399851.2:n.856-127_856-126del
ENST00000631044.2:c.*239-127_*239-126del	ENSP00000486730.1:n.*239-127_*239-126del
NM_001126131.1:c.856-127_856-126del	NP_001119603.1:n.856-127_856-126del
NM_002693.2:c.856-127_856-126del	NP_002684.1:n.856-127_856-126del
NM_001126131.2:c.856-127_856-126del	NP_001119603.1:n.856-127_856-126del
NM_002693.3:c.856-127_856-126del MANE Select	NP_002684.1:n.856-127_856-126del