Canonical Allele Identifier: CA492076349

Gene: POLG

Linked Data

• MyVariant Identifiers: chr15:g.89866665A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.89323434A>C , CM000677.2:g.89323434A>C	GRCh38
NC_000015.9:g.89866665A>C , CM000677.1:g.89866665A>C	GRCh37
NC_000015.8:g.87667669A>C	NCBI36
NG_008218.1:g.16362T>G
NG_008218.2:g.16362T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000636937.2:c.2235T>G	ENSP00000516154.1:p.Pro745=
ENST00000268124.11:c.2235T>G MANE Select	ENSP00000268124.5:p.Pro745=
ENST00000530292.3:c.1836T>G	ENSP00000432885.2:p.Pro612=
ENST00000635986.2:c.2235T>G	ENSP00000490653.2:p.Pro745=
ENST00000636774.1:c.*802T>G	ENSP00000489799.1:n.*802T>G
ENST00000637238.1:c.932T>G	ENSP00000490756.1:n.932T>G
ENST00000637264.1:c.1307T>G
ENST00000666746.1:c.1812T>G
ENST00000670281.1:c.555T>G	ENSP00000499709.1:p.Pro185=
ENST00000672071.1:n.2433T>G
ENST00000672923.2:n.2338T>G
ENST00000268124.9:c.2235T>G	ENSP00000268124.5:p.Pro745=
ENST00000442287.6:c.2235T>G	ENSP00000399851.2:p.Pro745=
ENST00000526314.2:c.539+381T>G
ENST00000526398.1:c.384T>G
ENST00000528881.2:c.4T>G
ENST00000532584.5:n.437T>G
ENST00000631044.2:c.*1659T>G	ENSP00000486730.1:n.*1659T>G
NM_001126131.1:c.2235T>G	NP_001119603.1:p.Pro745=
NM_002693.2:c.2235T>G	NP_002684.1:p.Pro745=
NM_001126131.2:c.2235T>G	NP_001119603.1:p.Pro745=
NM_002693.3:c.2235T>G MANE Select	NP_002684.1:p.Pro745=