Canonical Allele Identifier: CA393751130

Gene: POLG

Linked Data

• MyVariant Identifiers: chr15:g.89862307A>T (hg19) ; chr15:g.89319076A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.89319076A>T , CM000677.2:g.89319076A>T	GRCh38
NC_000015.9:g.89862307A>T , CM000677.1:g.89862307A>T	GRCh37
NC_000015.8:g.87663311A>T	NCBI36
NG_008218.1:g.20720T>A
NG_011736.1:g.80114A>T , LRG_500:g.80114A>T
NG_008218.2:g.20720T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000636937.2:c.3128T>A	ENSP00000516154.1:p.Val1043Glu
ENST00000268124.11:c.3128T>A MANE Select	ENSP00000268124.5:p.Val1043Glu
ENST00000530292.3:c.2729T>A	ENSP00000432885.2:p.Val910Glu
ENST00000635986.2:c.*198T>A	ENSP00000490653.2:n.*198T>A
ENST00000636530.1:n.88T>A
ENST00000636774.1:c.*1695T>A	ENSP00000489799.1:n.*1695T>A
ENST00000637238.1:c.1937T>A	ENSP00000490756.1:n.1937T>A
ENST00000637264.1:c.2200T>A
ENST00000666746.1:c.2705T>A
ENST00000672071.1:n.3326T>A
ENST00000672695.1:n.305T>A
ENST00000672923.2:n.3128T>A
ENST00000268124.9:c.3128T>A	ENSP00000268124.5:p.Val1043Glu
ENST00000442287.6:c.3128T>A	ENSP00000399851.2:p.Val1043Glu
ENST00000530292.2:c.212T>A	ENSP00000432885.1:p.Val71Glu
ENST00000631044.2:c.*2552T>A	ENSP00000486730.1:n.*2552T>A
NM_001126131.1:c.3128T>A	NP_001119603.1:p.Val1043Glu
NM_002693.2:c.3128T>A	NP_002684.1:p.Val1043Glu
NM_001126131.2:c.3128T>A	NP_001119603.1:p.Val1043Glu
NM_002693.3:c.3128T>A MANE Select	NP_002684.1:p.Val1043Glu