Canonical Allele Identifier: CA393754322

Gene: POLG

Linked Data

• MyVariant Identifiers: chr15:g.89864996G>T (hg19) ; chr15:g.89321765G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.89321765G>T , CM000677.2:g.89321765G>T	GRCh38
NC_000015.9:g.89864996G>T , CM000677.1:g.89864996G>T	GRCh37
NC_000015.8:g.87666000G>T	NCBI36
NG_008218.1:g.18031C>A
NG_008218.2:g.18031C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000636937.2:c.2569C>A	ENSP00000516154.1:p.Pro857Thr
ENST00000268124.11:c.2569C>A MANE Select	ENSP00000268124.5:p.Pro857Thr
ENST00000530292.3:c.2170C>A	ENSP00000432885.2:p.Pro724Thr
ENST00000635986.2:c.2569C>A	ENSP00000490653.2:p.Pro857Thr
ENST00000636774.1:c.*1136C>A	ENSP00000489799.1:n.*1136C>A
ENST00000637238.1:c.1266C>A	ENSP00000490756.1:n.1266C>A
ENST00000637264.1:c.1641C>A
ENST00000666746.1:c.2146C>A
ENST00000670281.1:c.800+197C>A	ENSP00000499709.1:n.800+197C>A
ENST00000672071.1:n.2767C>A
ENST00000672923.2:n.2511C>A
ENST00000268124.9:c.2569C>A	ENSP00000268124.5:p.Pro857Thr
ENST00000442287.6:c.2569C>A	ENSP00000399851.2:p.Pro857Thr
ENST00000528881.2:c.196-505C>A
ENST00000530715.5:c.186-896C>A	ENSP00000431395.1:n.186-896C>A
ENST00000631044.2:c.*1993C>A	ENSP00000486730.1:n.*1993C>A
NM_001126131.1:c.2569C>A	NP_001119603.1:p.Pro857Thr
NM_002693.2:c.2569C>A	NP_002684.1:p.Pro857Thr
NM_001126131.2:c.2569C>A	NP_001119603.1:p.Pro857Thr
NM_002693.3:c.2569C>A MANE Select	NP_002684.1:p.Pro857Thr