Canonical Allele Identifier: CA393753039

Gene: POLG

Linked Data

• MyVariant Identifiers: chr15:g.89864174G>C (hg19) ; chr15:g.89320943G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.89320943G>C , CM000677.2:g.89320943G>C	GRCh38
NC_000015.9:g.89864174G>C , CM000677.1:g.89864174G>C	GRCh37
NC_000015.8:g.87665178G>C	NCBI36
NG_008218.1:g.18853C>G
NG_008218.2:g.18853C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000636937.2:c.2804C>G	ENSP00000516154.1:p.Thr935Arg
ENST00000268124.11:c.2804C>G MANE Select	ENSP00000268124.5:p.Thr935Arg
ENST00000530292.3:c.2405C>G	ENSP00000432885.2:p.Thr802Arg
ENST00000635986.2:c.2804C>G	ENSP00000490653.2:p.Thr935Arg
ENST00000636774.1:c.*1371C>G	ENSP00000489799.1:n.*1371C>G
ENST00000637238.1:c.1613C>G	ENSP00000490756.1:n.1613C>G
ENST00000637264.1:c.1876C>G
ENST00000666746.1:c.2381C>G
ENST00000670281.1:c.800+1019C>G	ENSP00000499709.1:n.800+1019C>G
ENST00000672071.1:n.3002C>G
ENST00000672923.2:n.2746C>G
ENST00000268124.9:c.2804C>G	ENSP00000268124.5:p.Thr935Arg
ENST00000442287.6:c.2804C>G	ENSP00000399851.2:p.Thr935Arg
ENST00000528881.2:c.401C>G
ENST00000530715.5:c.186-74C>G	ENSP00000431395.1:n.186-74C>G
ENST00000631044.2:c.*2228C>G	ENSP00000486730.1:n.*2228C>G
NM_001126131.1:c.2804C>G	NP_001119603.1:p.Thr935Arg
NM_002693.2:c.2804C>G	NP_002684.1:p.Thr935Arg
NM_001126131.2:c.2804C>G	NP_001119603.1:p.Thr935Arg
NM_002693.3:c.2804C>G MANE Select	NP_002684.1:p.Thr935Arg