Canonical Allele Identifier: CA7725022

Gene: POLG

Linked Data

• dbSNP Id: rs755745614
• ExAC: 15:89873272 A / ATC
• gnomAD v4: 15-89330041-A-ATC
• MyVariant Identifiers: chr15:g.89873272_89873273insTC (hg19) ; chr15:g.89330041_89330042insTC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.89330042_89330043dup , CM000677.2:g.89330042_89330043dup	GRCh38
NC_000015.9:g.89873273_89873274dup , CM000677.1:g.89873273_89873274dup	GRCh37
NC_000015.8:g.87674277_87674278dup	NCBI36
NG_008218.1:g.9753_9754dup
NG_008218.2:g.9753_9754dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000636937.2:c.855+38_855+39dup	ENSP00000516154.1:n.855+38_855+39dup
ENST00000268124.11:c.855+38_855+39dup MANE Select	ENSP00000268124.5:n.855+38_855+39dup
ENST00000530292.3:c.456+38_456+39dup	ENSP00000432885.2:n.456+38_456+39dup
ENST00000635986.2:c.855+38_855+39dup	ENSP00000490653.2:n.855+38_855+39dup
ENST00000636774.1:c.855+38_855+39dup	ENSP00000489799.1:n.855+38_855+39dup
ENST00000666746.1:c.512+38_512+39dup
ENST00000672071.1:n.1053+38_1053+39dup
ENST00000268124.9:c.855+38_855+39dup	ENSP00000268124.5:n.855+38_855+39dup
ENST00000442287.6:c.855+38_855+39dup	ENSP00000399851.2:n.855+38_855+39dup
ENST00000631044.2:c.*238+38_*238+39dup	ENSP00000486730.1:n.*238+38_*238+39dup
NM_001126131.1:c.855+38_855+39dup	NP_001119603.1:n.855+38_855+39dup
NM_002693.2:c.855+38_855+39dup	NP_002684.1:n.855+38_855+39dup
NM_001126131.2:c.855+38_855+39dup	NP_001119603.1:n.855+38_855+39dup
NM_002693.3:c.855+38_855+39dup MANE Select	NP_002684.1:n.855+38_855+39dup