Canonical Allele Identifier: CA393761544

Gene: POLG

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.89327182A>G , CM000677.2:g.89327182A>G	GRCh38
NC_000015.9:g.89870413A>G , CM000677.1:g.89870413A>G	GRCh37
NC_000015.8:g.87671417A>G	NCBI36
NG_008218.1:g.12614T>C
NG_008218.2:g.12614T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_002693.3:c.1418T>C MANE Select	NP_002684.1:p.Leu473Pro
ENST00000268124.11:c.1418T>C MANE Select	ENSP00000268124.5:p.Leu473Pro
NM_001126131.1:c.1418T>C	NP_001119603.1:p.Leu473Pro
NM_001126131.2:c.1418T>C	NP_001119603.1:p.Leu473Pro
NM_002693.2:c.1418T>C	NP_002684.1:p.Leu473Pro
ENST00000268124.9:c.1418T>C	ENSP00000268124.5:p.Leu473Pro
ENST00000442287.6:c.1418T>C	ENSP00000399851.2:p.Leu473Pro
ENST00000530292.3:c.1019T>C	ENSP00000432885.2:p.Leu340Pro
ENST00000532363.2:n.276T>C
ENST00000631044.2:c.*801T>C	ENSP00000486730.1:n.*801T>C
ENST00000635986.2:c.1418T>C	ENSP00000490653.2:p.Leu473Pro
ENST00000636774.1:c.1418T>C	ENSP00000489799.1:p.Leu473Pro
ENST00000636937.2:c.1418T>C	ENSP00000516154.1:p.Leu473Pro
ENST00000637238.1:c.155T>C	ENSP00000490756.1:p.Leu52Pro
ENST00000637264.1:c.490T>C
ENST00000666746.1:c.995T>C
ENST00000672071.1:n.1616T>C
ENST00000672923.2:n.1521T>C