Canonical Allele Identifier: CA492070566

Gene: POLG

Linked Data

• MyVariant Identifiers: chr15:g.89860656T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.89317425T>C , CM000677.2:g.89317425T>C	GRCh38
NC_000015.9:g.89860656T>C , CM000677.1:g.89860656T>C	GRCh37
NC_000015.8:g.87661660T>C	NCBI36
NG_008218.1:g.22371A>G
NG_011736.1:g.78463T>C , LRG_500:g.78463T>C
NG_008218.2:g.22371A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000636937.2:c.3594A>G	ENSP00000516154.1:p.Lys1198=
ENST00000268124.11:c.3594A>G MANE Select	ENSP00000268124.5:p.Lys1198=
ENST00000530292.3:c.3294A>G	ENSP00000432885.2:n.3294A>G
ENST00000635986.2:c.*664A>G	ENSP00000490653.2:n.*664A>G
ENST00000636774.1:c.*2198A>G	ENSP00000489799.1:n.*2198A>G
ENST00000637238.1:c.2502A>G	ENSP00000490756.1:n.2502A>G
ENST00000637264.1:c.2606A>G
ENST00000666746.1:c.3171A>G
ENST00000672071.1:n.4796A>G
ENST00000672695.1:n.1373A>G
ENST00000672923.2:n.3594A>G
ENST00000268124.9:c.3594A>G	ENSP00000268124.5:p.Lys1198=
ENST00000442287.6:c.3594A>G	ENSP00000399851.2:p.Lys1198=
ENST00000526671.1:n.404A>G
ENST00000530292.2:c.777A>G	ENSP00000432885.1:n.777A>G
ENST00000631044.2:c.*3018A>G	ENSP00000486730.1:n.*3018A>G
NM_001126131.1:c.3594A>G	NP_001119603.1:p.Lys1198=
NM_002693.2:c.3594A>G	NP_002684.1:p.Lys1198=
NM_001126131.2:c.3594A>G	NP_001119603.1:p.Lys1198=
NM_002693.3:c.3594A>G MANE Select	NP_002684.1:p.Lys1198=