Canonical Allele Identifier: CA393759269

Gene: POLG

Linked Data

• MyVariant Identifiers: chr15:g.89868798G>C (hg19) ; chr15:g.89325567G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.89325567G>C , CM000677.2:g.89325567G>C	GRCh38
NC_000015.9:g.89868798G>C , CM000677.1:g.89868798G>C	GRCh37
NC_000015.8:g.87669802G>C	NCBI36
NG_008218.1:g.14229C>G
NG_008218.2:g.14229C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000636937.2:c.1832C>G	ENSP00000516154.1:p.Pro611Arg
ENST00000268124.11:c.1832C>G MANE Select	ENSP00000268124.5:p.Pro611Arg
ENST00000530292.3:c.1433C>G	ENSP00000432885.2:p.Pro478Arg
ENST00000635986.2:c.1832C>G	ENSP00000490653.2:p.Pro611Arg
ENST00000636774.1:c.*399C>G	ENSP00000489799.1:n.*399C>G
ENST00000637238.1:c.569C>G	ENSP00000490756.1:p.Pro190Arg
ENST00000637264.1:c.904C>G
ENST00000666746.1:c.1409C>G
ENST00000670281.1:c.152C>G	ENSP00000499709.1:p.Pro51Arg
ENST00000672071.1:n.2030C>G
ENST00000672923.2:n.1935C>G
ENST00000268124.9:c.1832C>G	ENSP00000268124.5:p.Pro611Arg
ENST00000442287.6:c.1832C>G	ENSP00000399851.2:p.Pro611Arg
ENST00000526314.2:c.214C>G
ENST00000526398.1:c.21C>G
ENST00000532584.5:n.34C>G
ENST00000631044.2:c.*1215C>G	ENSP00000486730.1:n.*1215C>G
NM_001126131.1:c.1832C>G	NP_001119603.1:p.Pro611Arg
NM_002693.2:c.1832C>G	NP_002684.1:p.Pro611Arg
NM_001126131.2:c.1832C>G	NP_001119603.1:p.Pro611Arg
NM_002693.3:c.1832C>G MANE Select	NP_002684.1:p.Pro611Arg