Canonical Allele Identifier: CA492077902

Gene: POLG

Linked Data

• ClinVar Variation Id: 1147568
• ClinVar RCV Id: RCV001487137
• dbSNP Id: rs2055559518
• gnomAD v4: 15-89328958-G-A
• MyVariant Identifiers: chr15:g.89872189G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.89328958G>A , CM000677.2:g.89328958G>A	GRCh38
NC_000015.9:g.89872189G>A , CM000677.1:g.89872189G>A	GRCh37
NC_000015.8:g.87673193G>A	NCBI36
NG_008218.1:g.10838C>T
NG_008218.2:g.10838C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000636937.2:c.1008C>T	ENSP00000516154.1:p.Ala336=
ENST00000268124.11:c.1008C>T MANE Select	ENSP00000268124.5:p.Ala336=
ENST00000530292.3:c.609C>T	ENSP00000432885.2:p.Ala203=
ENST00000635986.2:c.1008C>T	ENSP00000490653.2:p.Ala336=
ENST00000636774.1:c.1008C>T	ENSP00000489799.1:p.Ala336=
ENST00000637264.1:c.80C>T
ENST00000666746.1:c.665C>T
ENST00000672071.1:n.1206C>T
ENST00000672923.2:n.5C>T
ENST00000268124.9:c.1008C>T	ENSP00000268124.5:p.Ala336=
ENST00000442287.6:c.1008C>T	ENSP00000399851.2:p.Ala336=
ENST00000631044.2:c.*391C>T	ENSP00000486730.1:n.*391C>T
NM_001126131.1:c.1008C>T	NP_001119603.1:p.Ala336=
NM_002693.2:c.1008C>T	NP_002684.1:p.Ala336=
NM_001126131.2:c.1008C>T	NP_001119603.1:p.Ala336=
NM_002693.3:c.1008C>T MANE Select	NP_002684.1:p.Ala336=