Canonical Allele Identifier: CA492070609

Gene: POLG

Linked Data

• gnomAD v4: 15-89317440-C-T
• MyVariant Identifiers: chr15:g.89860671C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.89317440C>T , CM000677.2:g.89317440C>T	GRCh38
NC_000015.9:g.89860671C>T , CM000677.1:g.89860671C>T	GRCh37
NC_000015.8:g.87661675C>T	NCBI36
NG_008218.1:g.22356G>A
NG_011736.1:g.78478C>T , LRG_500:g.78478C>T
NG_008218.2:g.22356G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000636937.2:c.3579G>A	ENSP00000516154.1:p.Val1193=
ENST00000268124.11:c.3579G>A MANE Select	ENSP00000268124.5:p.Val1193=
ENST00000530292.3:c.3279G>A	ENSP00000432885.2:n.3279G>A
ENST00000635986.2:c.*649G>A	ENSP00000490653.2:n.*649G>A
ENST00000636774.1:c.*2183G>A	ENSP00000489799.1:n.*2183G>A
ENST00000637238.1:c.2487G>A	ENSP00000490756.1:n.2487G>A
ENST00000637264.1:c.2591G>A
ENST00000666746.1:c.3156G>A
ENST00000672071.1:n.4781G>A
ENST00000672695.1:n.1358G>A
ENST00000672923.2:n.3579G>A
ENST00000268124.9:c.3579G>A	ENSP00000268124.5:p.Val1193=
ENST00000442287.6:c.3579G>A	ENSP00000399851.2:p.Val1193=
ENST00000526671.1:n.389G>A
ENST00000530292.2:c.762G>A	ENSP00000432885.1:n.762G>A
ENST00000631044.2:c.*3003G>A	ENSP00000486730.1:n.*3003G>A
NM_001126131.1:c.3579G>A	NP_001119603.1:p.Val1193=
NM_002693.2:c.3579G>A	NP_002684.1:p.Val1193=
NM_001126131.2:c.3579G>A	NP_001119603.1:p.Val1193=
NM_002693.3:c.3579G>A MANE Select	NP_002684.1:p.Val1193=