Canonical Allele Identifier: CA492289056

Gene: POLG

Linked Data

• MyVariant Identifiers: chr15:g.89862306C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.89319075C>G , CM000677.2:g.89319075C>G	GRCh38
NC_000015.9:g.89862306C>G , CM000677.1:g.89862306C>G	GRCh37
NC_000015.8:g.87663310C>G	NCBI36
NG_008218.1:g.20721G>C
NG_011736.1:g.80113C>G , LRG_500:g.80113C>G
NG_008218.2:g.20721G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000636937.2:c.3129G>C	ENSP00000516154.1:p.Val1043=
ENST00000268124.11:c.3129G>C MANE Select	ENSP00000268124.5:p.Val1043=
ENST00000530292.3:c.2730G>C	ENSP00000432885.2:p.Val910=
ENST00000635986.2:c.*199G>C	ENSP00000490653.2:n.*199G>C
ENST00000636530.1:n.89G>C
ENST00000636774.1:c.*1696G>C	ENSP00000489799.1:n.*1696G>C
ENST00000637238.1:c.1938G>C	ENSP00000490756.1:n.1938G>C
ENST00000637264.1:c.2201G>C
ENST00000666746.1:c.2706G>C
ENST00000672071.1:n.3327G>C
ENST00000672695.1:n.306G>C
ENST00000672923.2:n.3129G>C
ENST00000268124.9:c.3129G>C	ENSP00000268124.5:p.Val1043=
ENST00000442287.6:c.3129G>C	ENSP00000399851.2:p.Val1043=
ENST00000530292.2:c.213G>C	ENSP00000432885.1:p.Val71=
ENST00000631044.2:c.*2553G>C	ENSP00000486730.1:n.*2553G>C
NM_001126131.1:c.3129G>C	NP_001119603.1:p.Val1043=
NM_002693.2:c.3129G>C	NP_002684.1:p.Val1043=
NM_001126131.2:c.3129G>C	NP_001119603.1:p.Val1043=
NM_002693.3:c.3129G>C MANE Select	NP_002684.1:p.Val1043=