Canonical Allele Identifier: CA393761360

Gene: POLG

Linked Data

• MyVariant Identifiers: chr15:g.89870295C>T (hg19) ; chr15:g.89327064C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.89327064C>T , CM000677.2:g.89327064C>T	GRCh38
NC_000015.9:g.89870295C>T , CM000677.1:g.89870295C>T	GRCh37
NC_000015.8:g.87671299C>T	NCBI36
NG_008218.1:g.12732G>A
NG_008218.2:g.12732G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000636937.2:c.1434-1G>A	ENSP00000516154.1:n.1434-1G>A
ENST00000268124.11:c.1434-1G>A MANE Select	ENSP00000268124.5:n.1434-1G>A
ENST00000530292.3:c.1035-1G>A	ENSP00000432885.2:n.1035-1G>A
ENST00000635986.2:c.1434-1G>A	ENSP00000490653.2:n.1434-1G>A
ENST00000636774.1:c.1449G>A	ENSP00000489799.1:p.Ter483=
ENST00000637238.1:c.171-1G>A	ENSP00000490756.1:n.171-1G>A
ENST00000637264.1:c.506-1G>A
ENST00000666746.1:c.1011-1G>A
ENST00000672071.1:n.1632-1G>A
ENST00000672923.2:n.1537-1G>A
ENST00000268124.9:c.1434-1G>A	ENSP00000268124.5:n.1434-1G>A
ENST00000442287.6:c.1434-1G>A	ENSP00000399851.2:n.1434-1G>A
ENST00000532363.2:n.394G>A
ENST00000631044.2:c.*817-1G>A	ENSP00000486730.1:n.*817-1G>A
NM_001126131.1:c.1434-1G>A	NP_001119603.1:n.1434-1G>A
NM_002693.2:c.1434-1G>A	NP_002684.1:n.1434-1G>A
NM_001126131.2:c.1434-1G>A	NP_001119603.1:n.1434-1G>A
NM_002693.3:c.1434-1G>A MANE Select	NP_002684.1:n.1434-1G>A