Canonical Allele Identifier: CA492288850

Gene: POLG

Linked Data

• MyVariant Identifiers: chr15:g.89861966A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.89318735A>C , CM000677.2:g.89318735A>C	GRCh38
NC_000015.9:g.89861966A>C , CM000677.1:g.89861966A>C	GRCh37
NC_000015.8:g.87662970A>C	NCBI36
NG_008218.1:g.21061T>G
NG_011736.1:g.79773A>C , LRG_500:g.79773A>C
NG_008218.2:g.21061T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000636937.2:c.3288T>G	ENSP00000516154.1:p.Arg1096=
ENST00000268124.11:c.3288T>G MANE Select	ENSP00000268124.5:p.Arg1096=
ENST00000530292.3:c.2889T>G	ENSP00000432885.2:p.Arg963=
ENST00000635986.2:c.*358T>G	ENSP00000490653.2:n.*358T>G
ENST00000636774.1:c.*1855T>G	ENSP00000489799.1:n.*1855T>G
ENST00000637238.1:c.2097T>G	ENSP00000490756.1:n.2097T>G
ENST00000637264.1:c.2360T>G
ENST00000666746.1:c.2865T>G
ENST00000672071.1:n.3486T>G
ENST00000672695.1:n.465T>G
ENST00000672923.2:n.3288T>G
ENST00000268124.9:c.3288T>G	ENSP00000268124.5:p.Arg1096=
ENST00000442287.6:c.3288T>G	ENSP00000399851.2:p.Arg1096=
ENST00000530292.2:c.372T>G	ENSP00000432885.1:p.Arg124=
ENST00000631044.2:c.*2712T>G	ENSP00000486730.1:n.*2712T>G
NM_001126131.1:c.3288T>G	NP_001119603.1:p.Arg1096=
NM_002693.2:c.3288T>G	NP_002684.1:p.Arg1096=
NM_001126131.2:c.3288T>G	NP_001119603.1:p.Arg1096=
NM_002693.3:c.3288T>G MANE Select	NP_002684.1:p.Arg1096=