Canonical Allele Identifier: CA492289523

Gene: POLG

Linked Data

• gnomAD v4: 15-89325665-G-T
• MyVariant Identifiers: chr15:g.89868896G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.89325665G>T , CM000677.2:g.89325665G>T	GRCh38
NC_000015.9:g.89868896G>T , CM000677.1:g.89868896G>T	GRCh37
NC_000015.8:g.87669900G>T	NCBI36
NG_008218.1:g.14131C>A
NG_008218.2:g.14131C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000636937.2:c.1734C>A	ENSP00000516154.1:p.Pro578=
ENST00000268124.11:c.1734C>A MANE Select	ENSP00000268124.5:p.Pro578=
ENST00000530292.3:c.1335C>A	ENSP00000432885.2:p.Pro445=
ENST00000635986.2:c.1734C>A	ENSP00000490653.2:p.Pro578=
ENST00000636774.1:c.*301C>A	ENSP00000489799.1:n.*301C>A
ENST00000637238.1:c.471C>A	ENSP00000490756.1:p.Pro157=
ENST00000637264.1:c.806C>A
ENST00000666746.1:c.1311C>A
ENST00000670281.1:c.54C>A	ENSP00000499709.1:p.Pro18=
ENST00000672071.1:n.1932C>A
ENST00000672923.2:n.1837C>A
ENST00000268124.9:c.1734C>A	ENSP00000268124.5:p.Pro578=
ENST00000442287.6:c.1734C>A	ENSP00000399851.2:p.Pro578=
ENST00000526314.2:c.116C>A
ENST00000631044.2:c.*1117C>A	ENSP00000486730.1:n.*1117C>A
NM_001126131.1:c.1734C>A	NP_001119603.1:p.Pro578=
NM_002693.2:c.1734C>A	NP_002684.1:p.Pro578=
NM_001126131.2:c.1734C>A	NP_001119603.1:p.Pro578=
NM_002693.3:c.1734C>A MANE Select	NP_002684.1:p.Pro578=