Canonical Allele Identifier: CA393753081

Gene: POLG

Linked Data

• MyVariant Identifiers: chr15:g.89864181T>A (hg19) ; chr15:g.89320950T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.89320950T>A , CM000677.2:g.89320950T>A	GRCh38
NC_000015.9:g.89864181T>A , CM000677.1:g.89864181T>A	GRCh37
NC_000015.8:g.87665185T>A	NCBI36
NG_008218.1:g.18846A>T
NG_008218.2:g.18846A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000636937.2:c.2797A>T	ENSP00000516154.1:p.Ser933Cys
ENST00000268124.11:c.2797A>T MANE Select	ENSP00000268124.5:p.Ser933Cys
ENST00000530292.3:c.2398A>T	ENSP00000432885.2:p.Ser800Cys
ENST00000635986.2:c.2797A>T	ENSP00000490653.2:p.Ser933Cys
ENST00000636774.1:c.*1364A>T	ENSP00000489799.1:n.*1364A>T
ENST00000637238.1:c.1606A>T	ENSP00000490756.1:n.1606A>T
ENST00000637264.1:c.1869A>T
ENST00000666746.1:c.2374A>T
ENST00000670281.1:c.800+1012A>T	ENSP00000499709.1:n.800+1012A>T
ENST00000672071.1:n.2995A>T
ENST00000672923.2:n.2739A>T
ENST00000268124.9:c.2797A>T	ENSP00000268124.5:p.Ser933Cys
ENST00000442287.6:c.2797A>T	ENSP00000399851.2:p.Ser933Cys
ENST00000528881.2:c.394A>T
ENST00000530715.5:c.186-81A>T	ENSP00000431395.1:n.186-81A>T
ENST00000631044.2:c.*2221A>T	ENSP00000486730.1:n.*2221A>T
NM_001126131.1:c.2797A>T	NP_001119603.1:p.Ser933Cys
NM_002693.2:c.2797A>T	NP_002684.1:p.Ser933Cys
NM_001126131.2:c.2797A>T	NP_001119603.1:p.Ser933Cys
NM_002693.3:c.2797A>T MANE Select	NP_002684.1:p.Ser933Cys