Canonical Allele Identifier: CA393749866

Gene: POLG

Linked Data

• MyVariant Identifiers: chr15:g.89861880A>C (hg19) ; chr15:g.89318649A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.89318649A>C , CM000677.2:g.89318649A>C	GRCh38
NC_000015.9:g.89861880A>C , CM000677.1:g.89861880A>C	GRCh37
NC_000015.8:g.87662884A>C	NCBI36
NG_008218.1:g.21147T>G
NG_011736.1:g.79687A>C , LRG_500:g.79687A>C
NG_008218.2:g.21147T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000636937.2:c.3374T>G	ENSP00000516154.1:p.Ile1125Arg
ENST00000268124.11:c.3374T>G MANE Select	ENSP00000268124.5:p.Ile1125Arg
ENST00000530292.3:c.2975T>G	ENSP00000432885.2:p.Ile992Arg
ENST00000635986.2:c.*444T>G	ENSP00000490653.2:n.*444T>G
ENST00000636774.1:c.*1941T>G	ENSP00000489799.1:n.*1941T>G
ENST00000637238.1:c.2183T>G	ENSP00000490756.1:n.2183T>G
ENST00000637264.1:c.2446T>G
ENST00000666746.1:c.2951T>G
ENST00000672071.1:n.3572T>G
ENST00000672695.1:n.551T>G
ENST00000672923.2:n.3374T>G
ENST00000268124.9:c.3374T>G	ENSP00000268124.5:p.Ile1125Arg
ENST00000442287.6:c.3374T>G	ENSP00000399851.2:p.Ile1125Arg
ENST00000530292.2:c.458T>G	ENSP00000432885.1:p.Ile153Arg
ENST00000631044.2:c.*2798T>G	ENSP00000486730.1:n.*2798T>G
NM_001126131.1:c.3374T>G	NP_001119603.1:p.Ile1125Arg
NM_002693.2:c.3374T>G	NP_002684.1:p.Ile1125Arg
NM_001126131.2:c.3374T>G	NP_001119603.1:p.Ile1125Arg
NM_002693.3:c.3374T>G MANE Select	NP_002684.1:p.Ile1125Arg