Canonical Allele Identifier: CA656507320

Gene: POLG

Linked Data

• gnomAD v4: 15-89323552-C-A
• COSMIC: COSN1181728

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.89323552C>A , CM000677.2:g.89323552C>A	GRCh38
NC_000015.9:g.89866783C>A , CM000677.1:g.89866783C>A	GRCh37
NC_000015.8:g.87667787C>A	NCBI36
NG_008218.1:g.16244G>T
NG_008218.2:g.16244G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000636937.2:c.2158-41G>T	ENSP00000516154.1:n.2158-41G>T
ENST00000268124.11:c.2158-41G>T MANE Select	ENSP00000268124.5:n.2158-41G>T
ENST00000530292.3:c.1759-41G>T	ENSP00000432885.2:n.1759-41G>T
ENST00000635986.2:c.2158-41G>T	ENSP00000490653.2:n.2158-41G>T
ENST00000636774.1:c.*725-41G>T	ENSP00000489799.1:n.*725-41G>T
ENST00000637238.1:c.855-41G>T	ENSP00000490756.1:n.855-41G>T
ENST00000637264.1:c.1230-41G>T
ENST00000666746.1:c.1735-41G>T
ENST00000670281.1:c.478-41G>T	ENSP00000499709.1:n.478-41G>T
ENST00000672071.1:n.2356-41G>T
ENST00000672923.2:n.2261-41G>T
ENST00000268124.9:c.2158-41G>T	ENSP00000268124.5:n.2158-41G>T
ENST00000442287.6:c.2158-41G>T	ENSP00000399851.2:n.2158-41G>T
ENST00000526314.2:c.539+263G>T
ENST00000526398.1:c.307-41G>T
ENST00000526573.1:n.506G>T
ENST00000532584.5:n.360-41G>T
ENST00000533857.1:n.535G>T
ENST00000631044.2:c.*1541G>T	ENSP00000486730.1:n.*1541G>T
NM_001126131.1:c.2158-41G>T	NP_001119603.1:n.2158-41G>T
NM_002693.2:c.2158-41G>T	NP_002684.1:n.2158-41G>T
NM_001126131.2:c.2158-41G>T	NP_001119603.1:n.2158-41G>T
NM_002693.3:c.2158-41G>T MANE Select	NP_002684.1:n.2158-41G>T