Canonical Allele Identifier: CA492289174

Gene: POLG

Linked Data

• gnomAD v4: 15-89325455-G-T
• MyVariant Identifiers: chr15:g.89868686G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.89325455G>T , CM000677.2:g.89325455G>T	GRCh38
NC_000015.9:g.89868686G>T , CM000677.1:g.89868686G>T	GRCh37
NC_000015.8:g.87669690G>T	NCBI36
NG_008218.1:g.14341C>A
NG_008218.2:g.14341C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000636937.2:c.1944C>A	ENSP00000516154.1:p.Pro648=
ENST00000268124.11:c.1944C>A MANE Select	ENSP00000268124.5:p.Pro648=
ENST00000530292.3:c.1545C>A	ENSP00000432885.2:p.Pro515=
ENST00000635986.2:c.1944C>A	ENSP00000490653.2:p.Pro648=
ENST00000636774.1:c.*511C>A	ENSP00000489799.1:n.*511C>A
ENST00000637238.1:c.646+35C>A	ENSP00000490756.1:n.646+35C>A
ENST00000637264.1:c.1016C>A
ENST00000666746.1:c.1521C>A
ENST00000670281.1:c.264C>A	ENSP00000499709.1:p.Pro88=
ENST00000672071.1:n.2142C>A
ENST00000672923.2:n.2047C>A
ENST00000268124.9:c.1944C>A	ENSP00000268124.5:p.Pro648=
ENST00000442287.6:c.1944C>A	ENSP00000399851.2:p.Pro648=
ENST00000526314.2:c.326C>A
ENST00000526398.1:c.133C>A
ENST00000526573.1:n.30C>A
ENST00000532584.5:n.146C>A
ENST00000631044.2:c.*1327C>A	ENSP00000486730.1:n.*1327C>A
NM_001126131.1:c.1944C>A	NP_001119603.1:p.Pro648=
NM_002693.2:c.1944C>A	NP_002684.1:p.Pro648=
NM_001126131.2:c.1944C>A	NP_001119603.1:p.Pro648=
NM_002693.3:c.1944C>A MANE Select	NP_002684.1:p.Pro648=