Canonical Allele Identifier: CA2194543294
Gene: POLG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.89319083A= , CM000677.2:g.89319083A= GRCh38
NC_000015.9:g.89862314A= , CM000677.1:g.89862314A= GRCh37
NC_000015.8:g.87663318A= NCBI36
NG_008218.1:g.20713T=
NG_011736.1:g.80121A= , LRG_500:g.80121A=
NG_008218.2:g.20713T=

Transcript Alleles

HGVS Amino-acid change
ENST00000636937.2:c.3121T= ENSP00000516154.1:p.Trp1041=
ENST00000268124.11:c.3121T= MANE Select ENSP00000268124.5:p.Trp1041=
ENST00000530292.3:c.2722T= ENSP00000432885.2:p.Trp908=
ENST00000635986.2:c.*191T= ENSP00000490653.2:n.*191T=
ENST00000636530.1:n.81T=
ENST00000636774.1:c.*1688T= ENSP00000489799.1:n.*1688T=
ENST00000637238.1:c.1930T= ENSP00000490756.1:n.1930T=
ENST00000637264.1:c.2193T=
ENST00000666746.1:c.2698T=
ENST00000672071.1:n.3319T=
ENST00000672695.1:n.298T=
ENST00000672923.2:n.3121T=
ENST00000268124.9:c.3121T= ENSP00000268124.5:p.Trp1041=
ENST00000442287.6:c.3121T= ENSP00000399851.2:p.Trp1041=
ENST00000530292.2:c.205T= ENSP00000432885.1:p.Trp69=
ENST00000631044.2:c.*2545T= ENSP00000486730.1:n.*2545T=
NM_001126131.1:c.3121T= NP_001119603.1:p.Trp1041=
NM_002693.2:c.3121T= NP_002684.1:p.Trp1041=
NM_001126131.2:c.3121T= NP_001119603.1:p.Trp1041=
NM_002693.3:c.3121T= MANE Select NP_002684.1:p.Trp1041=