Canonical Allele Identifier: CA393756886

Gene: POLG

Linked Data

• MyVariant Identifiers: chr15:g.89866722C>A (hg19) ; chr15:g.89323491C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.89323491C>A , CM000677.2:g.89323491C>A	GRCh38
NC_000015.9:g.89866722C>A , CM000677.1:g.89866722C>A	GRCh37
NC_000015.8:g.87667726C>A	NCBI36
NG_008218.1:g.16305G>T
NG_008218.2:g.16305G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000636937.2:c.2178G>T	ENSP00000516154.1:p.Lys726Asn
ENST00000268124.11:c.2178G>T MANE Select	ENSP00000268124.5:p.Lys726Asn
ENST00000530292.3:c.1779G>T	ENSP00000432885.2:p.Lys593Asn
ENST00000635986.2:c.2178G>T	ENSP00000490653.2:p.Lys726Asn
ENST00000636774.1:c.*745G>T	ENSP00000489799.1:n.*745G>T
ENST00000637238.1:c.875G>T	ENSP00000490756.1:n.875G>T
ENST00000637264.1:c.1250G>T
ENST00000666746.1:c.1755G>T
ENST00000670281.1:c.498G>T	ENSP00000499709.1:p.Lys166Asn
ENST00000672071.1:n.2376G>T
ENST00000672923.2:n.2281G>T
ENST00000268124.9:c.2178G>T	ENSP00000268124.5:p.Lys726Asn
ENST00000442287.6:c.2178G>T	ENSP00000399851.2:p.Lys726Asn
ENST00000526314.2:c.539+324G>T
ENST00000526398.1:c.327G>T
ENST00000532584.5:n.380G>T
ENST00000631044.2:c.*1602G>T	ENSP00000486730.1:n.*1602G>T
NM_001126131.1:c.2178G>T	NP_001119603.1:p.Lys726Asn
NM_002693.2:c.2178G>T	NP_002684.1:p.Lys726Asn
NM_001126131.2:c.2178G>T	NP_001119603.1:p.Lys726Asn
NM_002693.3:c.2178G>T MANE Select	NP_002684.1:p.Lys726Asn