Canonical Allele Identifier: CA10602315

Gene: POLG

Linked Data

• ClinVar Variation Id: 619465
• ClinVar RCV Id: RCV000758516
• dbSNP Id: rs1567188293

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.89323528C>A , CM000677.2:g.89323528C>A	GRCh38
NC_000015.9:g.89866759C>A , CM000677.1:g.89866759C>A	GRCh37
NC_000015.8:g.87667763C>A	NCBI36
NG_008218.1:g.16268G>T
NG_008218.2:g.16268G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000636937.2:c.2158-17G>T	ENSP00000516154.1:n.2158-17G>T
ENST00000268124.11:c.2158-17G>T MANE Select	ENSP00000268124.5:n.2158-17G>T
ENST00000530292.3:c.1759-17G>T	ENSP00000432885.2:n.1759-17G>T
ENST00000635986.2:c.2158-17G>T	ENSP00000490653.2:n.2158-17G>T
ENST00000636774.1:c.*725-17G>T	ENSP00000489799.1:n.*725-17G>T
ENST00000637238.1:c.855-17G>T	ENSP00000490756.1:n.855-17G>T
ENST00000637264.1:c.1230-17G>T
ENST00000666746.1:c.1735-17G>T
ENST00000670281.1:c.478-17G>T	ENSP00000499709.1:n.478-17G>T
ENST00000672071.1:n.2356-17G>T
ENST00000672923.2:n.2261-17G>T
ENST00000268124.9:c.2158-17G>T	ENSP00000268124.5:n.2158-17G>T
ENST00000442287.6:c.2158-17G>T	ENSP00000399851.2:n.2158-17G>T
ENST00000526314.2:c.539+287G>T
ENST00000526398.1:c.307-17G>T
ENST00000526573.1:n.530G>T
ENST00000532584.5:n.360-17G>T
ENST00000533857.1:n.559G>T
ENST00000631044.2:c.*1565G>T	ENSP00000486730.1:n.*1565G>T
NM_001126131.1:c.2158-17G>T	NP_001119603.1:n.2158-17G>T
NM_002693.2:c.2158-17G>T	NP_002684.1:n.2158-17G>T
NM_001126131.2:c.2158-17G>T	NP_001119603.1:n.2158-17G>T
NM_002693.3:c.2158-17G>T MANE Select	NP_002684.1:n.2158-17G>T