Canonical Allele Identifier: CA393765101

Gene: POLG

Linked Data

• MyVariant Identifiers: chr15:g.89872033G>T (hg19) ; chr15:g.89328802G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.89328802G>T , CM000677.2:g.89328802G>T	GRCh38
NC_000015.9:g.89872033G>T , CM000677.1:g.89872033G>T	GRCh37
NC_000015.8:g.87673037G>T	NCBI36
NG_008218.1:g.10994C>A
NG_008218.2:g.10994C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000636937.2:c.1053C>A	ENSP00000516154.1:p.Ser351Arg
ENST00000268124.11:c.1053C>A MANE Select	ENSP00000268124.5:p.Ser351Arg
ENST00000530292.3:c.654C>A	ENSP00000432885.2:p.Ser218Arg
ENST00000635986.2:c.1053C>A	ENSP00000490653.2:p.Ser351Arg
ENST00000636774.1:c.1053C>A	ENSP00000489799.1:p.Ser351Arg
ENST00000637264.1:c.125C>A
ENST00000666746.1:c.710C>A
ENST00000672071.1:n.1251C>A
ENST00000672923.2:n.50C>A
ENST00000268124.9:c.1053C>A	ENSP00000268124.5:p.Ser351Arg
ENST00000442287.6:c.1053C>A	ENSP00000399851.2:p.Ser351Arg
ENST00000631044.2:c.*436C>A	ENSP00000486730.1:n.*436C>A
NM_001126131.1:c.1053C>A	NP_001119603.1:p.Ser351Arg
NM_002693.2:c.1053C>A	NP_002684.1:p.Ser351Arg
NM_001126131.2:c.1053C>A	NP_001119603.1:p.Ser351Arg
NM_002693.3:c.1053C>A MANE Select	NP_002684.1:p.Ser351Arg