Canonical Allele Identifier: CA2805168159

Gene: POLG

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.89329245_89329257del , CM000677.2:g.89329245_89329257del	GRCh38
NC_000015.9:g.89872476_89872488del , CM000677.1:g.89872476_89872488del	GRCh37
NC_000015.8:g.87673480_87673492del	NCBI36
NG_008218.1:g.10539_10551del
NG_008218.2:g.10539_10551del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000636937.2:c.856-147_856-135del	ENSP00000516154.1:n.856-147_856-135del
ENST00000268124.11:c.856-147_856-135del MANE Select	ENSP00000268124.5:n.856-147_856-135del
ENST00000530292.3:c.457-147_457-135del	ENSP00000432885.2:n.457-147_457-135del
ENST00000635986.2:c.856-147_856-135del	ENSP00000490653.2:n.856-147_856-135del
ENST00000636774.1:c.856-147_856-135del	ENSP00000489799.1:n.856-147_856-135del
ENST00000666746.1:c.513-147_513-135del
ENST00000672071.1:n.1054-147_1054-135del
ENST00000268124.9:c.856-147_856-135del	ENSP00000268124.5:n.856-147_856-135del
ENST00000442287.6:c.856-147_856-135del	ENSP00000399851.2:n.856-147_856-135del
ENST00000631044.2:c.*239-147_*239-135del	ENSP00000486730.1:n.*239-147_*239-135del
NM_001126131.1:c.856-147_856-135del	NP_001119603.1:n.856-147_856-135del
NM_002693.2:c.856-147_856-135del	NP_002684.1:n.856-147_856-135del
NM_001126131.2:c.856-147_856-135del	NP_001119603.1:n.856-147_856-135del
NM_002693.3:c.856-147_856-135del MANE Select	NP_002684.1:n.856-147_856-135del