Canonical Allele Identifier: CA393758926

Gene: POLG

Linked Data

• MyVariant Identifiers: chr15:g.89868689G>C (hg19) ; chr15:g.89325458G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.89325458G>C , CM000677.2:g.89325458G>C	GRCh38
NC_000015.9:g.89868689G>C , CM000677.1:g.89868689G>C	GRCh37
NC_000015.8:g.87669693G>C	NCBI36
NG_008218.1:g.14338C>G
NG_008218.2:g.14338C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000636937.2:c.1941C>G	ENSP00000516154.1:p.Cys647Trp
ENST00000268124.11:c.1941C>G MANE Select	ENSP00000268124.5:p.Cys647Trp
ENST00000530292.3:c.1542C>G	ENSP00000432885.2:p.Cys514Trp
ENST00000635986.2:c.1941C>G	ENSP00000490653.2:p.Cys647Trp
ENST00000636774.1:c.*508C>G	ENSP00000489799.1:n.*508C>G
ENST00000637238.1:c.646+32C>G	ENSP00000490756.1:n.646+32C>G
ENST00000637264.1:c.1013C>G
ENST00000666746.1:c.1518C>G
ENST00000670281.1:c.261C>G	ENSP00000499709.1:p.Cys87Trp
ENST00000672071.1:n.2139C>G
ENST00000672923.2:n.2044C>G
ENST00000268124.9:c.1941C>G	ENSP00000268124.5:p.Cys647Trp
ENST00000442287.6:c.1941C>G	ENSP00000399851.2:p.Cys647Trp
ENST00000526314.2:c.323C>G
ENST00000526398.1:c.130C>G
ENST00000526573.1:n.27C>G
ENST00000532584.5:n.143C>G
ENST00000631044.2:c.*1324C>G	ENSP00000486730.1:n.*1324C>G
NM_001126131.1:c.1941C>G	NP_001119603.1:p.Cys647Trp
NM_002693.2:c.1941C>G	NP_002684.1:p.Cys647Trp
NM_001126131.2:c.1941C>G	NP_001119603.1:p.Cys647Trp
NM_002693.3:c.1941C>G MANE Select	NP_002684.1:p.Cys647Trp