Canonical Allele Identifier: CA393759349

Gene: POLG

Linked Data

• MyVariant Identifiers: chr15:g.89868834G>T (hg19) ; chr15:g.89325603G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.89325603G>T , CM000677.2:g.89325603G>T	GRCh38
NC_000015.9:g.89868834G>T , CM000677.1:g.89868834G>T	GRCh37
NC_000015.8:g.87669838G>T	NCBI36
NG_008218.1:g.14193C>A
NG_008218.2:g.14193C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000636937.2:c.1796C>A	ENSP00000516154.1:p.Thr599Lys
ENST00000268124.11:c.1796C>A MANE Select	ENSP00000268124.5:p.Thr599Lys
ENST00000530292.3:c.1397C>A	ENSP00000432885.2:p.Thr466Lys
ENST00000635986.2:c.1796C>A	ENSP00000490653.2:p.Thr599Lys
ENST00000636774.1:c.*363C>A	ENSP00000489799.1:n.*363C>A
ENST00000637238.1:c.533C>A	ENSP00000490756.1:p.Thr178Lys
ENST00000637264.1:c.868C>A
ENST00000666746.1:c.1373C>A
ENST00000670281.1:c.116C>A	ENSP00000499709.1:p.Thr39Lys
ENST00000672071.1:n.1994C>A
ENST00000672923.2:n.1899C>A
ENST00000268124.9:c.1796C>A	ENSP00000268124.5:p.Thr599Lys
ENST00000442287.6:c.1796C>A	ENSP00000399851.2:p.Thr599Lys
ENST00000526314.2:c.178C>A
ENST00000631044.2:c.*1179C>A	ENSP00000486730.1:n.*1179C>A
NM_001126131.1:c.1796C>A	NP_001119603.1:p.Thr599Lys
NM_002693.2:c.1796C>A	NP_002684.1:p.Thr599Lys
NM_001126131.2:c.1796C>A	NP_001119603.1:p.Thr599Lys
NM_002693.3:c.1796C>A MANE Select	NP_002684.1:p.Thr599Lys