Canonical Allele Identifier: CA7724199

Gene: POLG

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.89318963G>A , CM000677.2:g.89318963G>A	GRCh38
NC_000015.9:g.89862194G>A , CM000677.1:g.89862194G>A	GRCh37
NC_000015.8:g.87663198G>A	NCBI36
NG_008218.1:g.20833C>T
NG_011736.1:g.80001G>A , LRG_500:g.80001G>A
NG_008218.2:g.20833C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_002693.3:c.3241C>T MANE Select	NP_002684.1:p.Arg1081Ter
ENST00000268124.11:c.3241C>T MANE Select	ENSP00000268124.5:p.Arg1081Ter
NM_001126131.1:c.3241C>T	NP_001119603.1:p.Arg1081Ter
NM_001126131.2:c.3241C>T	NP_001119603.1:p.Arg1081Ter
NM_002693.2:c.3241C>T	NP_002684.1:p.Arg1081Ter
ENST00000268124.9:c.3241C>T	ENSP00000268124.5:p.Arg1081Ter
ENST00000442287.6:c.3241C>T	ENSP00000399851.2:p.Arg1081Ter
ENST00000530292.2:c.325C>T	ENSP00000432885.1:p.Arg109Ter
ENST00000530292.3:c.2842C>T	ENSP00000432885.2:p.Arg948Ter
ENST00000631044.2:c.*2665C>T	ENSP00000486730.1:n.*2665C>T
ENST00000635986.2:c.*311C>T	ENSP00000490653.2:n.*311C>T
ENST00000636774.1:c.*1808C>T	ENSP00000489799.1:n.*1808C>T
ENST00000636937.2:c.3241C>T	ENSP00000516154.1:p.Arg1081Ter
ENST00000637238.1:c.2050C>T	ENSP00000490756.1:n.2050C>T
ENST00000637264.1:c.2313C>T
ENST00000666746.1:c.2818C>T
ENST00000672071.1:n.3439C>T
ENST00000672695.1:n.418C>T
ENST00000672923.2:n.3241C>T