Canonical Allele Identifier: CA393759074

Gene: POLG

Linked Data

• MyVariant Identifiers: chr15:g.89868724T>C (hg19) ; chr15:g.89325493T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.89325493T>C , CM000677.2:g.89325493T>C	GRCh38
NC_000015.9:g.89868724T>C , CM000677.1:g.89868724T>C	GRCh37
NC_000015.8:g.87669728T>C	NCBI36
NG_008218.1:g.14303A>G
NG_008218.2:g.14303A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000636937.2:c.1906A>G	ENSP00000516154.1:p.Thr636Ala
ENST00000268124.11:c.1906A>G MANE Select	ENSP00000268124.5:p.Thr636Ala
ENST00000530292.3:c.1507A>G	ENSP00000432885.2:p.Thr503Ala
ENST00000635986.2:c.1906A>G	ENSP00000490653.2:p.Thr636Ala
ENST00000636774.1:c.*473A>G	ENSP00000489799.1:n.*473A>G
ENST00000637238.1:c.643A>G	ENSP00000490756.1:p.Thr215Ala
ENST00000637264.1:c.978A>G
ENST00000666746.1:c.1483A>G
ENST00000670281.1:c.226A>G	ENSP00000499709.1:p.Thr76Ala
ENST00000672071.1:n.2104A>G
ENST00000672923.2:n.2009A>G
ENST00000268124.9:c.1906A>G	ENSP00000268124.5:p.Thr636Ala
ENST00000442287.6:c.1906A>G	ENSP00000399851.2:p.Thr636Ala
ENST00000526314.2:c.288A>G
ENST00000526398.1:c.95A>G
ENST00000532584.5:n.108A>G
ENST00000631044.2:c.*1289A>G	ENSP00000486730.1:n.*1289A>G
NM_001126131.1:c.1906A>G	NP_001119603.1:p.Thr636Ala
NM_002693.2:c.1906A>G	NP_002684.1:p.Thr636Ala
NM_001126131.2:c.1906A>G	NP_001119603.1:p.Thr636Ala
NM_002693.3:c.1906A>G MANE Select	NP_002684.1:p.Thr636Ala