Canonical Allele Identifier: CA393756693

Gene: POLG

Linked Data

• MyVariant Identifiers: chr15:g.89866667G>C (hg19) ; chr15:g.89323436G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.89323436G>C , CM000677.2:g.89323436G>C	GRCh38
NC_000015.9:g.89866667G>C , CM000677.1:g.89866667G>C	GRCh37
NC_000015.8:g.87667671G>C	NCBI36
NG_008218.1:g.16360C>G
NG_008218.2:g.16360C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000636937.2:c.2233C>G	ENSP00000516154.1:p.Pro745Ala
ENST00000268124.11:c.2233C>G MANE Select	ENSP00000268124.5:p.Pro745Ala
ENST00000530292.3:c.1834C>G	ENSP00000432885.2:p.Pro612Ala
ENST00000635986.2:c.2233C>G	ENSP00000490653.2:p.Pro745Ala
ENST00000636774.1:c.*800C>G	ENSP00000489799.1:n.*800C>G
ENST00000637238.1:c.930C>G	ENSP00000490756.1:n.930C>G
ENST00000637264.1:c.1305C>G
ENST00000666746.1:c.1810C>G
ENST00000670281.1:c.553C>G	ENSP00000499709.1:p.Pro185Ala
ENST00000672071.1:n.2431C>G
ENST00000672923.2:n.2336C>G
ENST00000268124.9:c.2233C>G	ENSP00000268124.5:p.Pro745Ala
ENST00000442287.6:c.2233C>G	ENSP00000399851.2:p.Pro745Ala
ENST00000526314.2:c.539+379C>G
ENST00000526398.1:c.382C>G
ENST00000528881.2:c.2C>G
ENST00000532584.5:n.435C>G
ENST00000631044.2:c.*1657C>G	ENSP00000486730.1:n.*1657C>G
NM_001126131.1:c.2233C>G	NP_001119603.1:p.Pro745Ala
NM_002693.2:c.2233C>G	NP_002684.1:p.Pro745Ala
NM_001126131.2:c.2233C>G	NP_001119603.1:p.Pro745Ala
NM_002693.3:c.2233C>G MANE Select	NP_002684.1:p.Pro745Ala