Canonical Allele Identifier: CA393759508

Gene: POLG

Linked Data

• MyVariant Identifiers: chr15:g.89868915C>A (hg19) ; chr15:g.89325684C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.89325684C>A , CM000677.2:g.89325684C>A	GRCh38
NC_000015.9:g.89868915C>A , CM000677.1:g.89868915C>A	GRCh37
NC_000015.8:g.87669919C>A	NCBI36
NG_008218.1:g.14112G>T
NG_008218.2:g.14112G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000636937.2:c.1715G>T	ENSP00000516154.1:p.Trp572Leu
ENST00000268124.11:c.1715G>T MANE Select	ENSP00000268124.5:p.Trp572Leu
ENST00000530292.3:c.1316G>T	ENSP00000432885.2:p.Trp439Leu
ENST00000635986.2:c.1715G>T	ENSP00000490653.2:p.Trp572Leu
ENST00000636774.1:c.*282G>T	ENSP00000489799.1:n.*282G>T
ENST00000637238.1:c.452G>T	ENSP00000490756.1:p.Trp151Leu
ENST00000637264.1:c.787G>T
ENST00000666746.1:c.1292G>T
ENST00000670281.1:c.35G>T	ENSP00000499709.1:p.Trp12Leu
ENST00000672071.1:n.1913G>T
ENST00000672923.2:n.1818G>T
ENST00000268124.9:c.1715G>T	ENSP00000268124.5:p.Trp572Leu
ENST00000442287.6:c.1715G>T	ENSP00000399851.2:p.Trp572Leu
ENST00000526314.2:c.97G>T
ENST00000631044.2:c.*1098G>T	ENSP00000486730.1:n.*1098G>T
NM_001126131.1:c.1715G>T	NP_001119603.1:p.Trp572Leu
NM_002693.2:c.1715G>T	NP_002684.1:p.Trp572Leu
NM_001126131.2:c.1715G>T	NP_001119603.1:p.Trp572Leu
NM_002693.3:c.1715G>T MANE Select	NP_002684.1:p.Trp572Leu