Canonical Allele Identifier: CA2575828383

Gene: POLG

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.89317298G>A , CM000677.2:g.89317298G>A	GRCh38
NC_000015.9:g.89860529G>A , CM000677.1:g.89860529G>A	GRCh37
NC_000015.8:g.87661533G>A	NCBI36
NG_008218.1:g.22498C>T
NG_011736.1:g.78336G>A , LRG_500:g.78336G>A
NG_008218.2:g.22498C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000636937.2:c.3643+78C>T	ENSP00000516154.1:n.3643+78C>T
ENST00000268124.11:c.3643+78C>T MANE Select	ENSP00000268124.5:n.3643+78C>T
ENST00000530292.3:c.3343+78C>T	ENSP00000432885.2:n.3343+78C>T
ENST00000635986.2:c.*713+78C>T	ENSP00000490653.2:n.*713+78C>T
ENST00000636774.1:c.*2247+78C>T	ENSP00000489799.1:n.*2247+78C>T
ENST00000637238.1:c.2551+78C>T	ENSP00000490756.1:n.2551+78C>T
ENST00000637264.1:c.2655+78C>T
ENST00000666746.1:c.3220+78C>T
ENST00000672071.1:n.4845+78C>T
ENST00000672695.1:n.1422+78C>T
ENST00000672923.2:n.3643+78C>T
ENST00000268124.9:c.3643+78C>T	ENSP00000268124.5:n.3643+78C>T
ENST00000442287.6:c.3643+78C>T	ENSP00000399851.2:n.3643+78C>T
ENST00000526671.1:n.453+78C>T
ENST00000530292.2:c.826+78C>T	ENSP00000432885.1:n.826+78C>T
ENST00000631044.2:c.*3067+78C>T	ENSP00000486730.1:n.*3067+78C>T
NM_001126131.1:c.3643+78C>T	NP_001119603.1:n.3643+78C>T
NM_002693.2:c.3643+78C>T	NP_002684.1:n.3643+78C>T
NM_001126131.2:c.3643+78C>T	NP_001119603.1:n.3643+78C>T
NM_002693.3:c.3643+78C>T MANE Select	NP_002684.1:n.3643+78C>T