Canonical Allele Identifier: CA972591892
Gene: POLG HGNC NCBI

Linked Data

dbSNP Id: rs200056162

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.89329122_89329127dup , CM000677.2:g.89329122_89329127dup GRCh38
NC_000015.9:g.89872353_89872358dup , CM000677.1:g.89872353_89872358dup GRCh37
NC_000015.8:g.87673357_87673362dup NCBI36
NG_008218.1:g.10678_10683dup
NG_008218.2:g.10678_10683dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000636937.2:c.856-8_856-3dup ENSP00000516154.1:n.856-8_856-3dup
ENST00000268124.11:c.856-8_856-3dup MANE Select ENSP00000268124.5:n.856-8_856-3dup
ENST00000530292.3:c.457-8_457-3dup ENSP00000432885.2:n.457-8_457-3dup
ENST00000635986.2:c.856-8_856-3dup ENSP00000490653.2:n.856-8_856-3dup
ENST00000636774.1:c.856-8_856-3dup ENSP00000489799.1:n.856-8_856-3dup
ENST00000666746.1:c.513-8_513-3dup
ENST00000672071.1:n.1054-8_1054-3dup
ENST00000268124.9:c.856-8_856-3dup ENSP00000268124.5:n.856-8_856-3dup
ENST00000442287.6:c.856-8_856-3dup ENSP00000399851.2:n.856-8_856-3dup
ENST00000631044.2:c.*239-8_*239-3dup ENSP00000486730.1:n.*239-8_*239-3dup
NM_001126131.1:c.856-8_856-3dup NP_001119603.1:n.856-8_856-3dup
NM_002693.2:c.856-8_856-3dup NP_002684.1:n.856-8_856-3dup
NM_001126131.2:c.856-8_856-3dup NP_001119603.1:n.856-8_856-3dup
NM_002693.3:c.856-8_856-3dup MANE Select NP_002684.1:n.856-8_856-3dup