Canonical Allele Identifier: CA2194565964
Gene: POLG HGNC NCBI
POLGARF HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.89330339C= , CM000677.2:g.89330339C= GRCh38
NC_000015.9:g.89873570C= , CM000677.1:g.89873570C= GRCh37
NC_000015.8:g.87674574C= NCBI36
NG_008218.1:g.9457G=
NG_008218.2:g.9457G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000636937.2:c.660-63G= (POLG) ENSP00000516154.1:n.660-63G=
ENST00000706918.1:c.715-63G= (POLGARF) ENSP00000516626.1:n.715-63G=
ENST00000268124.11:c.660-63G= (POLG) MANE Select ENSP00000268124.5:n.660-63G=
ENST00000530292.3:c.261-63G= (POLG) ENSP00000432885.2:n.261-63G=
ENST00000635986.2:c.660-63G= (POLG) ENSP00000490653.2:n.660-63G=
ENST00000636774.1:c.660-63G= (POLG) ENSP00000489799.1:n.660-63G=
ENST00000637307.1:c.50-78G= (POLG)
ENST00000650303.2:c.715-63G= (POLG) ENSP00000497242.2:n.715-63G=
ENST00000666746.1:c.317-63G= (POLG)
ENST00000672071.1:n.858-63G= (POLG)
ENST00000268124.9:c.660-63G= (POLG) ENSP00000268124.5:n.660-63G=
ENST00000442287.6:c.660-63G= (POLG) ENSP00000399851.2:n.660-63G=
ENST00000631044.2:c.*43-63G= (POLG) ENSP00000486730.1:n.*43-63G=
NM_001126131.1:c.660-63G= (POLG) NP_001119603.1:n.660-63G=
NM_002693.2:c.660-63G= (POLG) NP_002684.1:n.660-63G=
NM_001126131.2:c.660-63G= (POLG) NP_001119603.1:n.660-63G=
NM_002693.3:c.660-63G= (POLG) MANE Select NP_002684.1:n.660-63G=