Canonical Allele Identifier: CA393760825

Gene: POLG

Linked Data

• MyVariant Identifiers: chr15:g.89870206C>A (hg19) ; chr15:g.89326975C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.89326975C>A , CM000677.2:g.89326975C>A	GRCh38
NC_000015.9:g.89870206C>A , CM000677.1:g.89870206C>A	GRCh37
NC_000015.8:g.87671210C>A	NCBI36
NG_008218.1:g.12821G>T
NG_008218.2:g.12821G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000636937.2:c.1522G>T	ENSP00000516154.1:p.Ala508Ser
ENST00000268124.11:c.1522G>T MANE Select	ENSP00000268124.5:p.Ala508Ser
ENST00000530292.3:c.1123G>T	ENSP00000432885.2:p.Ala375Ser
ENST00000635986.2:c.1522G>T	ENSP00000490653.2:p.Ala508Ser
ENST00000636774.1:c.*89G>T	ENSP00000489799.1:n.*89G>T
ENST00000637238.1:c.259G>T	ENSP00000490756.1:p.Ala87Ser
ENST00000637264.1:c.594G>T
ENST00000666746.1:c.1099G>T
ENST00000672071.1:n.1720G>T
ENST00000672923.2:n.1625G>T
ENST00000268124.9:c.1522G>T	ENSP00000268124.5:p.Ala508Ser
ENST00000442287.6:c.1522G>T	ENSP00000399851.2:p.Ala508Ser
ENST00000631044.2:c.*905G>T	ENSP00000486730.1:n.*905G>T
NM_001126131.1:c.1522G>T	NP_001119603.1:p.Ala508Ser
NM_002693.2:c.1522G>T	NP_002684.1:p.Ala508Ser
NM_001126131.2:c.1522G>T	NP_001119603.1:p.Ala508Ser
NM_002693.3:c.1522G>T MANE Select	NP_002684.1:p.Ala508Ser