Canonical Allele Identifier: CA2575828930
Gene: POLG HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.89329203del , CM000677.2:g.89329203del GRCh38
NC_000015.9:g.89872434del , CM000677.1:g.89872434del GRCh37
NC_000015.8:g.87673438del NCBI36
NG_008218.1:g.10596del
NG_008218.2:g.10596del

Transcript Alleles

HGVS Amino-acid Change
ENST00000636937.2:c.856-90del ENSP00000516154.1:n.856-90del
ENST00000268124.11:c.856-90del MANE Select ENSP00000268124.5:n.856-90del
ENST00000530292.3:c.457-90del ENSP00000432885.2:n.457-90del
ENST00000635986.2:c.856-90del ENSP00000490653.2:n.856-90del
ENST00000636774.1:c.856-90del ENSP00000489799.1:n.856-90del
ENST00000666746.1:c.513-90del
ENST00000672071.1:n.1054-90del
ENST00000268124.9:c.856-90del ENSP00000268124.5:n.856-90del
ENST00000442287.6:c.856-90del ENSP00000399851.2:n.856-90del
ENST00000631044.2:c.*239-90del ENSP00000486730.1:n.*239-90del
NM_001126131.1:c.856-90del NP_001119603.1:n.856-90del
NM_002693.2:c.856-90del NP_002684.1:n.856-90del
NM_001126131.2:c.856-90del NP_001119603.1:n.856-90del
NM_002693.3:c.856-90del MANE Select NP_002684.1:n.856-90del