Canonical Allele Identifier: CA393754197

Gene: POLG

Linked Data

• MyVariant Identifiers: chr15:g.89864978T>G (hg19) ; chr15:g.89321747T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.89321747T>G , CM000677.2:g.89321747T>G	GRCh38
NC_000015.9:g.89864978T>G , CM000677.1:g.89864978T>G	GRCh37
NC_000015.8:g.87665982T>G	NCBI36
NG_008218.1:g.18049A>C
NG_008218.2:g.18049A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000636937.2:c.2587A>C	ENSP00000516154.1:p.Ser863Arg
ENST00000268124.11:c.2587A>C MANE Select	ENSP00000268124.5:p.Ser863Arg
ENST00000530292.3:c.2188A>C	ENSP00000432885.2:p.Ser730Arg
ENST00000635986.2:c.2587A>C	ENSP00000490653.2:p.Ser863Arg
ENST00000636774.1:c.*1154A>C	ENSP00000489799.1:n.*1154A>C
ENST00000637238.1:c.1284A>C	ENSP00000490756.1:n.1284A>C
ENST00000637264.1:c.1659A>C
ENST00000666746.1:c.2164A>C
ENST00000670281.1:c.800+215A>C	ENSP00000499709.1:n.800+215A>C
ENST00000672071.1:n.2785A>C
ENST00000672923.2:n.2529A>C
ENST00000268124.9:c.2587A>C	ENSP00000268124.5:p.Ser863Arg
ENST00000442287.6:c.2587A>C	ENSP00000399851.2:p.Ser863Arg
ENST00000528881.2:c.196-487A>C
ENST00000530715.5:c.186-878A>C	ENSP00000431395.1:n.186-878A>C
ENST00000631044.2:c.*2011A>C	ENSP00000486730.1:n.*2011A>C
NM_001126131.1:c.2587A>C	NP_001119603.1:p.Ser863Arg
NM_002693.2:c.2587A>C	NP_002684.1:p.Ser863Arg
NM_001126131.2:c.2587A>C	NP_001119603.1:p.Ser863Arg
NM_002693.3:c.2587A>C MANE Select	NP_002684.1:p.Ser863Arg