Canonical Allele Identifier: CA492076394

Gene: POLG

Linked Data

• gnomAD v4: 15-89323440-G-A
• MyVariant Identifiers: chr15:g.89866671G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.89323440G>A , CM000677.2:g.89323440G>A	GRCh38
NC_000015.9:g.89866671G>A , CM000677.1:g.89866671G>A	GRCh37
NC_000015.8:g.87667675G>A	NCBI36
NG_008218.1:g.16356C>T
NG_008218.2:g.16356C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000636937.2:c.2229C>T	ENSP00000516154.1:p.Asp743=
ENST00000268124.11:c.2229C>T MANE Select	ENSP00000268124.5:p.Asp743=
ENST00000530292.3:c.1830C>T	ENSP00000432885.2:p.Asp610=
ENST00000635986.2:c.2229C>T	ENSP00000490653.2:p.Asp743=
ENST00000636774.1:c.*796C>T	ENSP00000489799.1:n.*796C>T
ENST00000637238.1:c.926C>T	ENSP00000490756.1:n.926C>T
ENST00000637264.1:c.1301C>T
ENST00000666746.1:c.1806C>T
ENST00000670281.1:c.549C>T	ENSP00000499709.1:p.Asp183=
ENST00000672071.1:n.2427C>T
ENST00000672923.2:n.2332C>T
ENST00000268124.9:c.2229C>T	ENSP00000268124.5:p.Asp743=
ENST00000442287.6:c.2229C>T	ENSP00000399851.2:p.Asp743=
ENST00000526314.2:c.539+375C>T
ENST00000526398.1:c.378C>T
ENST00000532584.5:n.431C>T
ENST00000631044.2:c.*1653C>T	ENSP00000486730.1:n.*1653C>T
NM_001126131.1:c.2229C>T	NP_001119603.1:p.Asp743=
NM_002693.2:c.2229C>T	NP_002684.1:p.Asp743=
NM_001126131.2:c.2229C>T	NP_001119603.1:p.Asp743=
NM_002693.3:c.2229C>T MANE Select	NP_002684.1:p.Asp743=