Canonical Allele Identifier: CA492071473

Gene: POLG

Linked Data

• MyVariant Identifiers: chr15:g.89861810G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.89318579G>T , CM000677.2:g.89318579G>T	GRCh38
NC_000015.9:g.89861810G>T , CM000677.1:g.89861810G>T	GRCh37
NC_000015.8:g.87662814G>T	NCBI36
NG_008218.1:g.21217C>A
NG_011736.1:g.79617G>T , LRG_500:g.79617G>T
NG_008218.2:g.21217C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000636937.2:c.3444C>A	ENSP00000516154.1:p.Arg1148=
ENST00000268124.11:c.3444C>A MANE Select	ENSP00000268124.5:p.Arg1148=
ENST00000530292.3:c.3045C>A	ENSP00000432885.2:p.Arg1015=
ENST00000635986.2:c.*514C>A	ENSP00000490653.2:n.*514C>A
ENST00000636774.1:c.*2011C>A	ENSP00000489799.1:n.*2011C>A
ENST00000637238.1:c.2253C>A	ENSP00000490756.1:n.2253C>A
ENST00000637264.1:c.2516C>A
ENST00000666746.1:c.3021C>A
ENST00000672071.1:n.3642C>A
ENST00000672695.1:n.621C>A
ENST00000672923.2:n.3444C>A
ENST00000268124.9:c.3444C>A	ENSP00000268124.5:p.Arg1148=
ENST00000442287.6:c.3444C>A	ENSP00000399851.2:p.Arg1148=
ENST00000530292.2:c.528C>A	ENSP00000432885.1:p.Arg176=
ENST00000631044.2:c.*2868C>A	ENSP00000486730.1:n.*2868C>A
NM_001126131.1:c.3444C>A	NP_001119603.1:p.Arg1148=
NM_002693.2:c.3444C>A	NP_002684.1:p.Arg1148=
NM_001126131.2:c.3444C>A	NP_001119603.1:p.Arg1148=
NM_002693.3:c.3444C>A MANE Select	NP_002684.1:p.Arg1148=