Canonical Allele Identifier: CA7724974

Gene: POLG

Linked Data

• dbSNP Id: rs766830796
• ExAC: 15:89872126 AG / A
• gnomAD v2: 15-89872126-AG-A
• gnomAD v3: 15-89328895-AG-A
• gnomAD v4: 15-89328895-AG-A
• MyVariant Identifiers: chr15:g.89872127del (hg19) ; chr15:g.89328896del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.89328900del , CM000677.2:g.89328900del	GRCh38
NC_000015.9:g.89872131del , CM000677.1:g.89872131del	GRCh37
NC_000015.8:g.87673135del	NCBI36
NG_008218.1:g.10900del
NG_008218.2:g.10900del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000636937.2:c.1023+47del	ENSP00000516154.1:n.1023+47del
ENST00000268124.11:c.1023+47del MANE Select	ENSP00000268124.5:n.1023+47del
ENST00000530292.3:c.624+47del	ENSP00000432885.2:n.624+47del
ENST00000635986.2:c.1023+47del	ENSP00000490653.2:n.1023+47del
ENST00000636774.1:c.1023+47del	ENSP00000489799.1:n.1023+47del
ENST00000637264.1:c.95+47del
ENST00000666746.1:c.680+47del
ENST00000672071.1:n.1221+47del
ENST00000672923.2:n.20+47del
ENST00000268124.9:c.1023+47del	ENSP00000268124.5:n.1023+47del
ENST00000442287.6:c.1023+47del	ENSP00000399851.2:n.1023+47del
ENST00000631044.2:c.*406+47del	ENSP00000486730.1:n.*406+47del
NM_001126131.1:c.1023+47del	NP_001119603.1:n.1023+47del
NM_002693.2:c.1023+47del	NP_002684.1:n.1023+47del
NM_001126131.2:c.1023+47del	NP_001119603.1:n.1023+47del
NM_002693.3:c.1023+47del MANE Select	NP_002684.1:n.1023+47del