Canonical Allele Identifier: CA393753089

Gene: POLG

Linked Data

• MyVariant Identifiers: chr15:g.89864183T>C (hg19) ; chr15:g.89320952T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.89320952T>C , CM000677.2:g.89320952T>C	GRCh38
NC_000015.9:g.89864183T>C , CM000677.1:g.89864183T>C	GRCh37
NC_000015.8:g.87665187T>C	NCBI36
NG_008218.1:g.18844A>G
NG_008218.2:g.18844A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000636937.2:c.2795A>G	ENSP00000516154.1:p.His932Arg
ENST00000268124.11:c.2795A>G MANE Select	ENSP00000268124.5:p.His932Arg
ENST00000530292.3:c.2396A>G	ENSP00000432885.2:p.His799Arg
ENST00000635986.2:c.2795A>G	ENSP00000490653.2:p.His932Arg
ENST00000636774.1:c.*1362A>G	ENSP00000489799.1:n.*1362A>G
ENST00000637238.1:c.1604A>G	ENSP00000490756.1:n.1604A>G
ENST00000637264.1:c.1867A>G
ENST00000666746.1:c.2372A>G
ENST00000670281.1:c.800+1010A>G	ENSP00000499709.1:n.800+1010A>G
ENST00000672071.1:n.2993A>G
ENST00000672923.2:n.2737A>G
ENST00000268124.9:c.2795A>G	ENSP00000268124.5:p.His932Arg
ENST00000442287.6:c.2795A>G	ENSP00000399851.2:p.His932Arg
ENST00000528881.2:c.392A>G
ENST00000530715.5:c.186-83A>G	ENSP00000431395.1:n.186-83A>G
ENST00000631044.2:c.*2219A>G	ENSP00000486730.1:n.*2219A>G
NM_001126131.1:c.2795A>G	NP_001119603.1:p.His932Arg
NM_002693.2:c.2795A>G	NP_002684.1:p.His932Arg
NM_001126131.2:c.2795A>G	NP_001119603.1:p.His932Arg
NM_002693.3:c.2795A>G MANE Select	NP_002684.1:p.His932Arg