Canonical Allele Identifier: CA2194541656
Gene: POLG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.89318582G= , CM000677.2:g.89318582G= GRCh38
NC_000015.9:g.89861813G= , CM000677.1:g.89861813G= GRCh37
NC_000015.8:g.87662817G= NCBI36
NG_008218.1:g.21214C=
NG_011736.1:g.79620G= , LRG_500:g.79620G=
NG_008218.2:g.21214C=

Transcript Alleles

HGVS Amino-acid change
ENST00000636937.2:c.3441C= ENSP00000516154.1:p.Tyr1147=
ENST00000268124.11:c.3441C= MANE Select ENSP00000268124.5:p.Tyr1147=
ENST00000530292.3:c.3042C= ENSP00000432885.2:p.Tyr1014=
ENST00000635986.2:c.*511C= ENSP00000490653.2:n.*511C=
ENST00000636774.1:c.*2008C= ENSP00000489799.1:n.*2008C=
ENST00000637238.1:c.2250C= ENSP00000490756.1:n.2250C=
ENST00000637264.1:c.2513C=
ENST00000666746.1:c.3018C=
ENST00000672071.1:n.3639C=
ENST00000672695.1:n.618C=
ENST00000672923.2:n.3441C=
ENST00000268124.9:c.3441C= ENSP00000268124.5:p.Tyr1147=
ENST00000442287.6:c.3441C= ENSP00000399851.2:p.Tyr1147=
ENST00000530292.2:c.525C= ENSP00000432885.1:p.Tyr175=
ENST00000631044.2:c.*2865C= ENSP00000486730.1:n.*2865C=
NM_001126131.1:c.3441C= NP_001119603.1:p.Tyr1147=
NM_002693.2:c.3441C= NP_002684.1:p.Tyr1147=
NM_001126131.2:c.3441C= NP_001119603.1:p.Tyr1147=
NM_002693.3:c.3441C= MANE Select NP_002684.1:p.Tyr1147=