Canonical Allele Identifier: CA919614165
Gene: POLG HGNC NCBI

Linked Data

dbSNP Id: rs1555453840

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.89329116_89329117insT , CM000677.2:g.89329116_89329117insT GRCh38
NC_000015.9:g.89872347_89872348insT , CM000677.1:g.89872347_89872348insT GRCh37
NC_000015.8:g.87673351_87673352insT NCBI36
NG_008218.1:g.10679_10680insA
NG_008218.2:g.10679_10680insA

Transcript Alleles

HGVS Amino-acid Change
ENST00000636937.2:c.856-7_856-6insA ENSP00000516154.1:n.856-7_856-6insA
ENST00000268124.11:c.856-7_856-6insA MANE Select ENSP00000268124.5:n.856-7_856-6insA
ENST00000530292.3:c.457-7_457-6insA ENSP00000432885.2:n.457-7_457-6insA
ENST00000635986.2:c.856-7_856-6insA ENSP00000490653.2:n.856-7_856-6insA
ENST00000636774.1:c.856-7_856-6insA ENSP00000489799.1:n.856-7_856-6insA
ENST00000666746.1:c.513-7_513-6insA
ENST00000672071.1:n.1054-7_1054-6insA
ENST00000268124.9:c.856-7_856-6insA ENSP00000268124.5:n.856-7_856-6insA
ENST00000442287.6:c.856-7_856-6insA ENSP00000399851.2:n.856-7_856-6insA
ENST00000631044.2:c.*239-7_*239-6insA ENSP00000486730.1:n.*239-7_*239-6insA
NM_001126131.1:c.856-7_856-6insA NP_001119603.1:n.856-7_856-6insA
NM_002693.2:c.856-7_856-6insA NP_002684.1:n.856-7_856-6insA
NM_001126131.2:c.856-7_856-6insA NP_001119603.1:n.856-7_856-6insA
NM_002693.3:c.856-7_856-6insA MANE Select NP_002684.1:n.856-7_856-6insA