Canonical Allele Identifier: CA492289051

Gene: POLG

Linked Data

• MyVariant Identifiers: chr15:g.89862303A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.89319072A>T , CM000677.2:g.89319072A>T	GRCh38
NC_000015.9:g.89862303A>T , CM000677.1:g.89862303A>T	GRCh37
NC_000015.8:g.87663307A>T	NCBI36
NG_008218.1:g.20724T>A
NG_011736.1:g.80110A>T , LRG_500:g.80110A>T
NG_008218.2:g.20724T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000636937.2:c.3132T>A	ENSP00000516154.1:p.Val1044=
ENST00000268124.11:c.3132T>A MANE Select	ENSP00000268124.5:p.Val1044=
ENST00000530292.3:c.2733T>A	ENSP00000432885.2:p.Val911=
ENST00000635986.2:c.*202T>A	ENSP00000490653.2:n.*202T>A
ENST00000636530.1:n.92T>A
ENST00000636774.1:c.*1699T>A	ENSP00000489799.1:n.*1699T>A
ENST00000637238.1:c.1941T>A	ENSP00000490756.1:n.1941T>A
ENST00000637264.1:c.2204T>A
ENST00000666746.1:c.2709T>A
ENST00000672071.1:n.3330T>A
ENST00000672695.1:n.309T>A
ENST00000672923.2:n.3132T>A
ENST00000268124.9:c.3132T>A	ENSP00000268124.5:p.Val1044=
ENST00000442287.6:c.3132T>A	ENSP00000399851.2:p.Val1044=
ENST00000530292.2:c.216T>A	ENSP00000432885.1:p.Val72=
ENST00000631044.2:c.*2556T>A	ENSP00000486730.1:n.*2556T>A
NM_001126131.1:c.3132T>A	NP_001119603.1:p.Val1044=
NM_002693.2:c.3132T>A	NP_002684.1:p.Val1044=
NM_001126131.2:c.3132T>A	NP_001119603.1:p.Val1044=
NM_002693.3:c.3132T>A MANE Select	NP_002684.1:p.Val1044=