Canonical Allele Identifier: CA1139664123

Gene: POLG

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.89328545G>C , CM000677.2:g.89328545G>C	GRCh38
NC_000015.9:g.89871776G>C , CM000677.1:g.89871776G>C	GRCh37
NC_000015.8:g.87672780G>C	NCBI36
NG_008218.1:g.11251C>G
NG_008218.2:g.11251C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_002693.3:c.1171-10C>G MANE Select	NP_002684.1:n.1171-10C>G
ENST00000268124.11:c.1171-10C>G MANE Select	ENSP00000268124.5:n.1171-10C>G
NM_001126131.1:c.1171-10C>G	NP_001119603.1:n.1171-10C>G
NM_001126131.2:c.1171-10C>G	NP_001119603.1:n.1171-10C>G
NM_002693.2:c.1171-10C>G	NP_002684.1:n.1171-10C>G
ENST00000268124.9:c.1171-10C>G	ENSP00000268124.5:n.1171-10C>G
ENST00000442287.6:c.1171-10C>G	ENSP00000399851.2:n.1171-10C>G
ENST00000530292.3:c.772-10C>G	ENSP00000432885.2:n.772-10C>G
ENST00000532363.2:n.29-10C>G
ENST00000631044.2:c.*554-10C>G	ENSP00000486730.1:n.*554-10C>G
ENST00000635986.2:c.1171-10C>G	ENSP00000490653.2:n.1171-10C>G
ENST00000636774.1:c.1171-10C>G	ENSP00000489799.1:n.1171-10C>G
ENST00000636937.2:c.1171-10C>G	ENSP00000516154.1:n.1171-10C>G
ENST00000637264.1:c.243-10C>G
ENST00000666746.1:c.827+140C>G
ENST00000672071.1:n.1369-10C>G
ENST00000672923.2:n.168-10C>G