Canonical Allele Identifier: CA2630254869

Gene: POLG

Linked Data

• gnomAD v4: 15-89317310-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.89317310C>T , CM000677.2:g.89317310C>T	GRCh38
NC_000015.9:g.89860541C>T , CM000677.1:g.89860541C>T	GRCh37
NC_000015.8:g.87661545C>T	NCBI36
NG_008218.1:g.22486G>A
NG_011736.1:g.78348C>T , LRG_500:g.78348C>T
NG_008218.2:g.22486G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000636937.2:c.3643+66G>A	ENSP00000516154.1:n.3643+66G>A
ENST00000268124.11:c.3643+66G>A MANE Select	ENSP00000268124.5:n.3643+66G>A
ENST00000530292.3:c.3343+66G>A	ENSP00000432885.2:n.3343+66G>A
ENST00000635986.2:c.*713+66G>A	ENSP00000490653.2:n.*713+66G>A
ENST00000636774.1:c.*2247+66G>A	ENSP00000489799.1:n.*2247+66G>A
ENST00000637238.1:c.2551+66G>A	ENSP00000490756.1:n.2551+66G>A
ENST00000637264.1:c.2655+66G>A
ENST00000666746.1:c.3220+66G>A
ENST00000672071.1:n.4845+66G>A
ENST00000672695.1:n.1422+66G>A
ENST00000672923.2:n.3643+66G>A
ENST00000268124.9:c.3643+66G>A	ENSP00000268124.5:n.3643+66G>A
ENST00000442287.6:c.3643+66G>A	ENSP00000399851.2:n.3643+66G>A
ENST00000526671.1:n.453+66G>A
ENST00000530292.2:c.826+66G>A	ENSP00000432885.1:n.826+66G>A
ENST00000631044.2:c.*3067+66G>A	ENSP00000486730.1:n.*3067+66G>A
NM_001126131.1:c.3643+66G>A	NP_001119603.1:n.3643+66G>A
NM_002693.2:c.3643+66G>A	NP_002684.1:n.3643+66G>A
NM_001126131.2:c.3643+66G>A	NP_001119603.1:n.3643+66G>A
NM_002693.3:c.3643+66G>A MANE Select	NP_002684.1:n.3643+66G>A