Canonical Allele Identifier: CA393759327

Gene: POLG

Linked Data

• MyVariant Identifiers: chr15:g.89868823T>C (hg19) ; chr15:g.89325592T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.89325592T>C , CM000677.2:g.89325592T>C	GRCh38
NC_000015.9:g.89868823T>C , CM000677.1:g.89868823T>C	GRCh37
NC_000015.8:g.87669827T>C	NCBI36
NG_008218.1:g.14204A>G
NG_008218.2:g.14204A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000636937.2:c.1807A>G	ENSP00000516154.1:p.Met603Val
ENST00000268124.11:c.1807A>G MANE Select	ENSP00000268124.5:p.Met603Val
ENST00000530292.3:c.1408A>G	ENSP00000432885.2:p.Met470Val
ENST00000635986.2:c.1807A>G	ENSP00000490653.2:p.Met603Val
ENST00000636774.1:c.*374A>G	ENSP00000489799.1:n.*374A>G
ENST00000637238.1:c.544A>G	ENSP00000490756.1:p.Met182Val
ENST00000637264.1:c.879A>G
ENST00000666746.1:c.1384A>G
ENST00000670281.1:c.127A>G	ENSP00000499709.1:p.Met43Val
ENST00000672071.1:n.2005A>G
ENST00000672923.2:n.1910A>G
ENST00000268124.9:c.1807A>G	ENSP00000268124.5:p.Met603Val
ENST00000442287.6:c.1807A>G	ENSP00000399851.2:p.Met603Val
ENST00000526314.2:c.189A>G
ENST00000532584.5:n.9A>G
ENST00000631044.2:c.*1190A>G	ENSP00000486730.1:n.*1190A>G
NM_001126131.1:c.1807A>G	NP_001119603.1:p.Met603Val
NM_002693.2:c.1807A>G	NP_002684.1:p.Met603Val
NM_001126131.2:c.1807A>G	NP_001119603.1:p.Met603Val
NM_002693.3:c.1807A>G MANE Select	NP_002684.1:p.Met603Val