Canonical Allele Identifier: CA972590098

Gene: POLG

Linked Data

• gnomAD v3: 15-89325301-T-TGAGTGAGAGAGTGAGTGAGTGAGTGAGAGAGTGA
• gnomAD v4: 15-89325301-T-TGAGTGAGAGAGTGAGTGAGTGAGTGAGAGAGTGA

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.89325302_89325303insAGTGAGAGAGTGAGTGAGTGAGTGAGAGAGTGAG , CM000677.2:g.89325302_89325303insAGTGAGAGAGTGAGTGAGTGAGTGAGAGAGTGAG	GRCh38
NC_000015.9:g.89868533_89868534insAGTGAGAGAGTGAGTGAGTGAGTGAGAGAGTGAG , CM000677.1:g.89868533_89868534insAGTGAGAGAGTGAGTGAGTGAGTGAGAGAGTGAG	GRCh37
NC_000015.8:g.87669537_87669538insAGTGAGAGAGTGAGTGAGTGAGTGAGAGAGTGAG	NCBI36
NG_008218.1:g.14494_14495insTCACTCTCTCACTCACTCACTCACTCTCTCACTC
NG_008218.2:g.14494_14495insTCACTCTCTCACTCACTCACTCACTCTCTCACTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000636937.2:c.1949+148_1949+149insTCACTCTCTCACTCACTCACTCACTCTCTCACTC	ENSP00000516154.1:n.1949+148_1949+149insTCACTCTCTCACTCACTCACT...
ENST00000268124.11:c.1949+148_1949+149insTCACTCTCTCACTCACTCACTCACTCTCTCACTC MANE Select	ENSP00000268124.5:n.1949+148_1949+149insTCACTCTCTCACTCACTCACT...
ENST00000530292.3:c.1550+148_1550+149insTCACTCTCTCACTCACTCACTCACTCTCTCACTC	ENSP00000432885.2:n.1550+148_1550+149insTCACTCTCTCACTCACTCACT...
ENST00000635986.2:c.1949+148_1949+149insTCACTCTCTCACTCACTCACTCACTCTCTCACTC	ENSP00000490653.2:n.1949+148_1949+149insTCACTCTCTCACTCACTCACT...
ENST00000636774.1:c.*516+148_*516+149insTCACTCTCTCACTCACTCACTCACTCTCTCACTC	ENSP00000489799.1:n.*516+148_*516+149insTCACTCTCTCACTCACTCACT...
ENST00000637238.1:c.646+188_646+189insTCACTCTCTCACTCACTCACTCACTCTCTCACTC	ENSP00000490756.1:n.646+188_646+189insTCACTCTCTCACTCACTCACTCA...
ENST00000637264.1:c.1021+148_1021+149insTCACTCTCTCACTCACTCACTCACTCTCTCACTC
ENST00000666746.1:c.1526+148_1526+149insTCACTCTCTCACTCACTCACTCACTCTCTCACTC
ENST00000670281.1:c.269+148_269+149insTCACTCTCTCACTCACTCACTCACTCTCTCACTC	ENSP00000499709.1:n.269+148_269+149insTCACTCTCTCACTCACTCACTCA...
ENST00000672071.1:n.2147+148_2147+149insTCACTCTCTCACTCACTCACTCACTCTCTCACTC
ENST00000672923.2:n.2052+148_2052+149insTCACTCTCTCACTCACTCACTCACTCTCTCACTC
ENST00000268124.9:c.1949+148_1949+149insTCACTCTCTCACTCACTCACTCACTCTCTCACTC	ENSP00000268124.5:n.1949+148_1949+149insTCACTCTCTCACTCACTCACT...
ENST00000442287.6:c.1949+148_1949+149insTCACTCTCTCACTCACTCACTCACTCTCTCACTC	ENSP00000399851.2:n.1949+148_1949+149insTCACTCTCTCACTCACTCACT...
ENST00000526314.2:c.331+148_331+149insTCACTCTCTCACTCACTCACTCACTCTCTCACTC
ENST00000526398.1:c.138+148_138+149insTCACTCTCTCACTCACTCACTCACTCTCTCACTC
ENST00000526573.1:n.35+148_35+149insTCACTCTCTCACTCACTCACTCACTCTCTCACTC
ENST00000532584.5:n.151+148_151+149insTCACTCTCTCACTCACTCACTCACTCTCTCACTC
ENST00000631044.2:c.*1332+148_*1332+149insTCACTCTCTCACTCACTCACTCACTCTCTCACTC	ENSP00000486730.1:n.*1332+148_*1332+149insTCACTCTCTCACTCACTCA...
NM_001126131.1:c.1949+148_1949+149insTCACTCTCTCACTCACTCACTCACTCTCTCACTC	NP_001119603.1:n.1949+148_1949+149insTCACTCTCTCACTCACTCACTCAC...
NM_002693.2:c.1949+148_1949+149insTCACTCTCTCACTCACTCACTCACTCTCTCACTC	NP_002684.1:n.1949+148_1949+149insTCACTCTCTCACTCACTCACTCACTCT...
NM_001126131.2:c.1949+148_1949+149insTCACTCTCTCACTCACTCACTCACTCTCTCACTC	NP_001119603.1:n.1949+148_1949+149insTCACTCTCTCACTCACTCACTCAC...
NM_002693.3:c.1949+148_1949+149insTCACTCTCTCACTCACTCACTCACTCTCTCACTC MANE Select	NP_002684.1:n.1949+148_1949+149insTCACTCTCTCACTCACTCACTCACTCT...