Canonical Allele Identifier: CA393748027
Gene: POLG HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.89317510A>T , CM000677.2:g.89317510A>T GRCh38
NC_000015.9:g.89860741A>T , CM000677.1:g.89860741A>T GRCh37
NC_000015.8:g.87661745A>T NCBI36
NG_008218.1:g.22286T>A
NG_011736.1:g.78548A>T , LRG_500:g.78548A>T
NG_008218.2:g.22286T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000636937.2:c.3509T>A ENSP00000516154.1:p.Leu1170Gln
ENST00000268124.11:c.3509T>A MANE Select ENSP00000268124.5:p.Leu1170Gln
ENST00000530292.3:c.3209T>A ENSP00000432885.2:n.3209T>A
ENST00000635986.2:c.*579T>A ENSP00000490653.2:n.*579T>A
ENST00000636774.1:c.*2113T>A ENSP00000489799.1:n.*2113T>A
ENST00000637042.1:n.72-39T>A
ENST00000637238.1:c.2417T>A ENSP00000490756.1:n.2417T>A
ENST00000637264.1:c.2555-34T>A
ENST00000666746.1:c.3086T>A
ENST00000672071.1:n.4711T>A
ENST00000672695.1:n.1288T>A
ENST00000672923.2:n.3509T>A
ENST00000268124.9:c.3509T>A ENSP00000268124.5:p.Leu1170Gln
ENST00000442287.6:c.3509T>A ENSP00000399851.2:p.Leu1170Gln
ENST00000526671.1:n.319T>A
ENST00000530292.2:c.692T>A ENSP00000432885.1:n.692T>A
ENST00000631044.2:c.*2933T>A ENSP00000486730.1:n.*2933T>A
NM_001126131.1:c.3509T>A NP_001119603.1:p.Leu1170Gln
NM_002693.2:c.3509T>A NP_002684.1:p.Leu1170Gln
NM_001126131.2:c.3509T>A NP_001119603.1:p.Leu1170Gln
NM_002693.3:c.3509T>A MANE Select NP_002684.1:p.Leu1170Gln