Canonical Allele Identifier: CA393766887

Gene: POLG

Linked Data

• COSMIC: COSM3741725
• MyVariant Identifiers: chr15:g.89873384C>T (hg19) ; chr15:g.89330153C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.89330153C>T , CM000677.2:g.89330153C>T	GRCh38
NC_000015.9:g.89873384C>T , CM000677.1:g.89873384C>T	GRCh37
NC_000015.8:g.87674388C>T	NCBI36
NG_008218.1:g.9643G>A
NG_008218.2:g.9643G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000636937.2:c.783G>A	ENSP00000516154.1:p.Trp261Ter
ENST00000268124.11:c.783G>A MANE Select	ENSP00000268124.5:p.Trp261Ter
ENST00000530292.3:c.384G>A	ENSP00000432885.2:p.Trp128Ter
ENST00000635986.2:c.783G>A	ENSP00000490653.2:p.Trp261Ter
ENST00000636774.1:c.783G>A	ENSP00000489799.1:p.Trp261Ter
ENST00000666746.1:c.440G>A
ENST00000672071.1:n.981G>A
ENST00000268124.9:c.783G>A	ENSP00000268124.5:p.Trp261Ter
ENST00000442287.6:c.783G>A	ENSP00000399851.2:p.Trp261Ter
ENST00000631044.2:c.*166G>A	ENSP00000486730.1:n.*166G>A
NM_001126131.1:c.783G>A	NP_001119603.1:p.Trp261Ter
NM_002693.2:c.783G>A	NP_002684.1:p.Trp261Ter
NM_001126131.2:c.783G>A	NP_001119603.1:p.Trp261Ter
NM_002693.3:c.783G>A MANE Select	NP_002684.1:p.Trp261Ter