Canonical Allele Identifier: CA492289803

Gene: POLG

Linked Data

• MyVariant Identifiers: chr15:g.89871982G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.89328751G>T , CM000677.2:g.89328751G>T	GRCh38
NC_000015.9:g.89871982G>T , CM000677.1:g.89871982G>T	GRCh37
NC_000015.8:g.87672986G>T	NCBI36
NG_008218.1:g.11045C>A
NG_008218.2:g.11045C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000636937.2:c.1104C>A	ENSP00000516154.1:p.Pro368=
ENST00000268124.11:c.1104C>A MANE Select	ENSP00000268124.5:p.Pro368=
ENST00000530292.3:c.705C>A	ENSP00000432885.2:p.Pro235=
ENST00000635986.2:c.1104C>A	ENSP00000490653.2:p.Pro368=
ENST00000636774.1:c.1104C>A	ENSP00000489799.1:p.Pro368=
ENST00000637264.1:c.176C>A
ENST00000666746.1:c.761C>A
ENST00000672071.1:n.1302C>A
ENST00000672923.2:n.101C>A
ENST00000268124.9:c.1104C>A	ENSP00000268124.5:p.Pro368=
ENST00000442287.6:c.1104C>A	ENSP00000399851.2:p.Pro368=
ENST00000631044.2:c.*487C>A	ENSP00000486730.1:n.*487C>A
NM_001126131.1:c.1104C>A	NP_001119603.1:p.Pro368=
NM_002693.2:c.1104C>A	NP_002684.1:p.Pro368=
NM_001126131.2:c.1104C>A	NP_001119603.1:p.Pro368=
NM_002693.3:c.1104C>A MANE Select	NP_002684.1:p.Pro368=