Canonical Allele Identifier: CA393754159

Gene: POLG

Linked Data

• MyVariant Identifiers: chr15:g.89864972C>T (hg19) ; chr15:g.89321741C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.89321741C>T , CM000677.2:g.89321741C>T	GRCh38
NC_000015.9:g.89864972C>T , CM000677.1:g.89864972C>T	GRCh37
NC_000015.8:g.87665976C>T	NCBI36
NG_008218.1:g.18055G>A
NG_008218.2:g.18055G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000636937.2:c.2593G>A	ENSP00000516154.1:p.Ala865Thr
ENST00000268124.11:c.2593G>A MANE Select	ENSP00000268124.5:p.Ala865Thr
ENST00000530292.3:c.2194G>A	ENSP00000432885.2:p.Ala732Thr
ENST00000635986.2:c.2593G>A	ENSP00000490653.2:p.Ala865Thr
ENST00000636774.1:c.*1160G>A	ENSP00000489799.1:n.*1160G>A
ENST00000637238.1:c.1290G>A	ENSP00000490756.1:n.1290G>A
ENST00000637264.1:c.1665G>A
ENST00000666746.1:c.2170G>A
ENST00000670281.1:c.800+221G>A	ENSP00000499709.1:n.800+221G>A
ENST00000672071.1:n.2791G>A
ENST00000672923.2:n.2535G>A
ENST00000268124.9:c.2593G>A	ENSP00000268124.5:p.Ala865Thr
ENST00000442287.6:c.2593G>A	ENSP00000399851.2:p.Ala865Thr
ENST00000528881.2:c.196-481G>A
ENST00000530715.5:c.186-872G>A	ENSP00000431395.1:n.186-872G>A
ENST00000631044.2:c.*2017G>A	ENSP00000486730.1:n.*2017G>A
NM_001126131.1:c.2593G>A	NP_001119603.1:p.Ala865Thr
NM_002693.2:c.2593G>A	NP_002684.1:p.Ala865Thr
NM_001126131.2:c.2593G>A	NP_001119603.1:p.Ala865Thr
NM_002693.3:c.2593G>A MANE Select	NP_002684.1:p.Ala865Thr