Canonical Allele Identifier: CA393751210

Gene: POLG

Linked Data

• MyVariant Identifiers: chr15:g.89862321C>G (hg19) ; chr15:g.89319090C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.89319090C>G , CM000677.2:g.89319090C>G	GRCh38
NC_000015.9:g.89862321C>G , CM000677.1:g.89862321C>G	GRCh37
NC_000015.8:g.87663325C>G	NCBI36
NG_008218.1:g.20706G>C
NG_011736.1:g.80128C>G , LRG_500:g.80128C>G
NG_008218.2:g.20706G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000636937.2:c.3114G>C	ENSP00000516154.1:p.Trp1038Cys
ENST00000268124.11:c.3114G>C MANE Select	ENSP00000268124.5:p.Trp1038Cys
ENST00000530292.3:c.2715G>C	ENSP00000432885.2:p.Trp905Cys
ENST00000635986.2:c.*184G>C	ENSP00000490653.2:n.*184G>C
ENST00000636530.1:n.74G>C
ENST00000636774.1:c.*1681G>C	ENSP00000489799.1:n.*1681G>C
ENST00000637238.1:c.1923G>C	ENSP00000490756.1:n.1923G>C
ENST00000637264.1:c.2186G>C
ENST00000666746.1:c.2691G>C
ENST00000672071.1:n.3312G>C
ENST00000672695.1:n.291G>C
ENST00000672923.2:n.3114G>C
ENST00000268124.9:c.3114G>C	ENSP00000268124.5:p.Trp1038Cys
ENST00000442287.6:c.3114G>C	ENSP00000399851.2:p.Trp1038Cys
ENST00000530292.2:c.198G>C	ENSP00000432885.1:p.Trp66Cys
ENST00000631044.2:c.*2538G>C	ENSP00000486730.1:n.*2538G>C
NM_001126131.1:c.3114G>C	NP_001119603.1:p.Trp1038Cys
NM_002693.2:c.3114G>C	NP_002684.1:p.Trp1038Cys
NM_001126131.2:c.3114G>C	NP_001119603.1:p.Trp1038Cys
NM_002693.3:c.3114G>C MANE Select	NP_002684.1:p.Trp1038Cys