Canonical Allele Identifier: CA393756705

Gene: POLG

Linked Data

• MyVariant Identifiers: chr15:g.89866672T>C (hg19) ; chr15:g.89323441T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.89323441T>C , CM000677.2:g.89323441T>C	GRCh38
NC_000015.9:g.89866672T>C , CM000677.1:g.89866672T>C	GRCh37
NC_000015.8:g.87667676T>C	NCBI36
NG_008218.1:g.16355A>G
NG_008218.2:g.16355A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000636937.2:c.2228A>G	ENSP00000516154.1:p.Asp743Gly
ENST00000268124.11:c.2228A>G MANE Select	ENSP00000268124.5:p.Asp743Gly
ENST00000530292.3:c.1829A>G	ENSP00000432885.2:p.Asp610Gly
ENST00000635986.2:c.2228A>G	ENSP00000490653.2:p.Asp743Gly
ENST00000636774.1:c.*795A>G	ENSP00000489799.1:n.*795A>G
ENST00000637238.1:c.925A>G	ENSP00000490756.1:n.925A>G
ENST00000637264.1:c.1300A>G
ENST00000666746.1:c.1805A>G
ENST00000670281.1:c.548A>G	ENSP00000499709.1:p.Asp183Gly
ENST00000672071.1:n.2426A>G
ENST00000672923.2:n.2331A>G
ENST00000268124.9:c.2228A>G	ENSP00000268124.5:p.Asp743Gly
ENST00000442287.6:c.2228A>G	ENSP00000399851.2:p.Asp743Gly
ENST00000526314.2:c.539+374A>G
ENST00000526398.1:c.377A>G
ENST00000532584.5:n.430A>G
ENST00000631044.2:c.*1652A>G	ENSP00000486730.1:n.*1652A>G
NM_001126131.1:c.2228A>G	NP_001119603.1:p.Asp743Gly
NM_002693.2:c.2228A>G	NP_002684.1:p.Asp743Gly
NM_001126131.2:c.2228A>G	NP_001119603.1:p.Asp743Gly
NM_002693.3:c.2228A>G MANE Select	NP_002684.1:p.Asp743Gly