Canonical Allele Identifier: CA393754431

Gene: POLG

Linked Data

• MyVariant Identifiers: chr15:g.89865020T>G (hg19) ; chr15:g.89321789T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.89321789T>G , CM000677.2:g.89321789T>G	GRCh38
NC_000015.9:g.89865020T>G , CM000677.1:g.89865020T>G	GRCh37
NC_000015.8:g.87666024T>G	NCBI36
NG_008218.1:g.18007A>C
NG_008218.2:g.18007A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000636937.2:c.2545A>C	ENSP00000516154.1:p.Thr849Pro
ENST00000268124.11:c.2545A>C MANE Select	ENSP00000268124.5:p.Thr849Pro
ENST00000530292.3:c.2146A>C	ENSP00000432885.2:p.Thr716Pro
ENST00000635986.2:c.2545A>C	ENSP00000490653.2:p.Thr849Pro
ENST00000636774.1:c.*1112A>C	ENSP00000489799.1:n.*1112A>C
ENST00000637238.1:c.1242A>C	ENSP00000490756.1:n.1242A>C
ENST00000637264.1:c.1617A>C
ENST00000666746.1:c.2122A>C
ENST00000670281.1:c.800+173A>C	ENSP00000499709.1:n.800+173A>C
ENST00000672071.1:n.2743A>C
ENST00000672923.2:n.2487A>C
ENST00000268124.9:c.2545A>C	ENSP00000268124.5:p.Thr849Pro
ENST00000442287.6:c.2545A>C	ENSP00000399851.2:p.Thr849Pro
ENST00000528881.2:c.196-529A>C
ENST00000530715.5:c.186-920A>C	ENSP00000431395.1:n.186-920A>C
ENST00000532584.5:n.694A>C
ENST00000631044.2:c.*1969A>C	ENSP00000486730.1:n.*1969A>C
NM_001126131.1:c.2545A>C	NP_001119603.1:p.Thr849Pro
NM_002693.2:c.2545A>C	NP_002684.1:p.Thr849Pro
NM_001126131.2:c.2545A>C	NP_001119603.1:p.Thr849Pro
NM_002693.3:c.2545A>C MANE Select	NP_002684.1:p.Thr849Pro