Canonical Allele Identifier: CA393760719

Gene: POLG

Linked Data

• gnomAD v4: 15-89326920-T-A
• MyVariant Identifiers: chr15:g.89870151T>A (hg19) ; chr15:g.89326920T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.89326920T>A , CM000677.2:g.89326920T>A	GRCh38
NC_000015.9:g.89870151T>A , CM000677.1:g.89870151T>A	GRCh37
NC_000015.8:g.87671155T>A	NCBI36
NG_008218.1:g.12876A>T
NG_008218.2:g.12876A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000636937.2:c.1577A>T	ENSP00000516154.1:p.Asp526Val
ENST00000268124.11:c.1577A>T MANE Select	ENSP00000268124.5:p.Asp526Val
ENST00000530292.3:c.1178A>T	ENSP00000432885.2:p.Asp393Val
ENST00000635986.2:c.1577A>T	ENSP00000490653.2:p.Asp526Val
ENST00000636774.1:c.*144A>T	ENSP00000489799.1:n.*144A>T
ENST00000637238.1:c.314A>T	ENSP00000490756.1:p.Asp105Val
ENST00000637264.1:c.649A>T
ENST00000666746.1:c.1154A>T
ENST00000672071.1:n.1775A>T
ENST00000672923.2:n.1680A>T
ENST00000268124.9:c.1577A>T	ENSP00000268124.5:p.Asp526Val
ENST00000442287.6:c.1577A>T	ENSP00000399851.2:p.Asp526Val
ENST00000631044.2:c.*960A>T	ENSP00000486730.1:n.*960A>T
NM_001126131.1:c.1577A>T	NP_001119603.1:p.Asp526Val
NM_002693.2:c.1577A>T	NP_002684.1:p.Asp526Val
NM_001126131.2:c.1577A>T	NP_001119603.1:p.Asp526Val
NM_002693.3:c.1577A>T MANE Select	NP_002684.1:p.Asp526Val