Canonical Allele Identifier: CA393749987
Gene: POLG HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.89318697A>C , CM000677.2:g.89318697A>C GRCh38
NC_000015.9:g.89861928A>C , CM000677.1:g.89861928A>C GRCh37
NC_000015.8:g.87662932A>C NCBI36
NG_008218.1:g.21099T>G
NG_011736.1:g.79735A>C , LRG_500:g.79735A>C
NG_008218.2:g.21099T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000636937.2:c.3326T>G ENSP00000516154.1:p.Leu1109Ter
ENST00000268124.11:c.3326T>G MANE Select ENSP00000268124.5:p.Leu1109Ter
ENST00000530292.3:c.2927T>G ENSP00000432885.2:p.Leu976Ter
ENST00000635986.2:c.*396T>G ENSP00000490653.2:n.*396T>G
ENST00000636774.1:c.*1893T>G ENSP00000489799.1:n.*1893T>G
ENST00000637238.1:c.2135T>G ENSP00000490756.1:n.2135T>G
ENST00000637264.1:c.2398T>G
ENST00000666746.1:c.2903T>G
ENST00000672071.1:n.3524T>G
ENST00000672695.1:n.503T>G
ENST00000672923.2:n.3326T>G
ENST00000268124.9:c.3326T>G ENSP00000268124.5:p.Leu1109Ter
ENST00000442287.6:c.3326T>G ENSP00000399851.2:p.Leu1109Ter
ENST00000530292.2:c.410T>G ENSP00000432885.1:p.Leu137Ter
ENST00000631044.2:c.*2750T>G ENSP00000486730.1:n.*2750T>G
NM_001126131.1:c.3326T>G NP_001119603.1:p.Leu1109Ter
NM_002693.2:c.3326T>G NP_002684.1:p.Leu1109Ter
NM_001126131.2:c.3326T>G NP_001119603.1:p.Leu1109Ter
NM_002693.3:c.3326T>G MANE Select NP_002684.1:p.Leu1109Ter