Canonical Allele Identifier: CA393750109

Gene: POLG

Linked Data

• MyVariant Identifiers: chr15:g.89861949T>C (hg19) ; chr15:g.89318718T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.89318718T>C , CM000677.2:g.89318718T>C	GRCh38
NC_000015.9:g.89861949T>C , CM000677.1:g.89861949T>C	GRCh37
NC_000015.8:g.87662953T>C	NCBI36
NG_008218.1:g.21078A>G
NG_011736.1:g.79756T>C , LRG_500:g.79756T>C
NG_008218.2:g.21078A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000636937.2:c.3305A>G	ENSP00000516154.1:p.Gln1102Arg
ENST00000268124.11:c.3305A>G MANE Select	ENSP00000268124.5:p.Gln1102Arg
ENST00000530292.3:c.2906A>G	ENSP00000432885.2:p.Gln969Arg
ENST00000635986.2:c.*375A>G	ENSP00000490653.2:n.*375A>G
ENST00000636774.1:c.*1872A>G	ENSP00000489799.1:n.*1872A>G
ENST00000637238.1:c.2114A>G	ENSP00000490756.1:n.2114A>G
ENST00000637264.1:c.2377A>G
ENST00000666746.1:c.2882A>G
ENST00000672071.1:n.3503A>G
ENST00000672695.1:n.482A>G
ENST00000672923.2:n.3305A>G
ENST00000268124.9:c.3305A>G	ENSP00000268124.5:p.Gln1102Arg
ENST00000442287.6:c.3305A>G	ENSP00000399851.2:p.Gln1102Arg
ENST00000530292.2:c.389A>G	ENSP00000432885.1:p.Gln130Arg
ENST00000631044.2:c.*2729A>G	ENSP00000486730.1:n.*2729A>G
NM_001126131.1:c.3305A>G	NP_001119603.1:p.Gln1102Arg
NM_002693.2:c.3305A>G	NP_002684.1:p.Gln1102Arg
NM_001126131.2:c.3305A>G	NP_001119603.1:p.Gln1102Arg
NM_002693.3:c.3305A>G MANE Select	NP_002684.1:p.Gln1102Arg