Canonical Allele Identifier: CA492289975

Gene: POLG POLGARF

Linked Data

• gnomAD v4: 15-89333308-G-A
• MyVariant Identifiers: chr15:g.89876539G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.89333308G>A , CM000677.2:g.89333308G>A	GRCh38
NC_000015.9:g.89876539G>A , CM000677.1:g.89876539G>A	GRCh37
NC_000015.8:g.87677543G>A	NCBI36
NG_008218.1:g.6488C>T
NG_008218.2:g.6488C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000636937.2:c.447C>T (POLG)	ENSP00000516154.1:p.Pro149=
ENST00000706918.1:c.502C>T (POLGARF)	ENSP00000516626.1:p.Leu168=
ENST00000268124.11:c.447C>T (POLG) MANE Select	ENSP00000268124.5:p.Pro149=
ENST00000530292.3:c.48C>T (POLG)	ENSP00000432885.2:p.Pro16=
ENST00000635986.2:c.447C>T (POLG)	ENSP00000490653.2:p.Pro149=
ENST00000636774.1:c.447C>T (POLG)	ENSP00000489799.1:p.Pro149=
ENST00000650303.2:c.502C>T (POLG)	ENSP00000497242.2:p.Leu168=
ENST00000666746.1:c.104C>T (POLG)
ENST00000672071.1:n.645C>T (POLG)
ENST00000268124.9:c.447C>T (POLG)	ENSP00000268124.5:p.Pro149=
ENST00000442287.6:c.447C>T (POLG)	ENSP00000399851.2:p.Pro149=
ENST00000631044.2:c.447C>T (POLG)	ENSP00000486730.1:p.Pro149=
NM_001126131.1:c.447C>T (POLG)	NP_001119603.1:p.Pro149=
NM_002693.2:c.447C>T (POLG)	NP_002684.1:p.Pro149=
NM_001126131.2:c.447C>T (POLG)	NP_001119603.1:p.Pro149=
NM_002693.3:c.447C>T (POLG) MANE Select	NP_002684.1:p.Pro149=