Canonical Allele Identifier: CA619513851

Gene: POLG

Linked Data

• dbSNP Id: rs1567189709
• gnomAD v2: 15-89868408-AGAGAGTGAGTGAGTGAGAGAGTGAGTGAGAGAGTGAGTGAGTGAGAGAGTGAGTGAGAGAGTGAGTGAGTGAGAGAGAGAGTGAGTGAGTGAGTGAGAGAGAGAGAAAG-A
• gnomAD v3: 15-89325177-AGAGAGTGAGTGAGTGAGAGAGTGAGTGAGAGAGTGAGTGAGTGAGAGAGTGAGTGAGAGAGTGAGTGAGTGAGAGAGAGAGTGAGTGAGTGAGTGAGAGAGAGAGAAAG-A
• gnomAD v4: 15-89325177-AGAGAGTGAGTGAGTGAGAGAGTGAGTGAGAGAGTGAGTGAGTGAGAGAGTGAGTGAGAGAGTGAGTGAGTGAGAGAGAGAGTGAGTGAGTGAGTGAGAGAGAGAGAAAG-A
• MyVariant Identifiers: chr15:g.89868409_89868517del (hg19) ; chr15:g.89325178_89325286del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.89325178_89325286del , CM000677.2:g.89325178_89325286del	GRCh38
NC_000015.9:g.89868409_89868517del , CM000677.1:g.89868409_89868517del	GRCh37
NC_000015.8:g.87669413_87669521del	NCBI36
NG_008218.1:g.14510_14618del
NG_008218.2:g.14510_14618del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000636937.2:c.1949+164_1949+272del	ENSP00000516154.1:n.1949+164_1949+272del
ENST00000268124.11:c.1949+164_1949+272del MANE Select	ENSP00000268124.5:n.1949+164_1949+272del
ENST00000530292.3:c.1550+164_1550+272del	ENSP00000432885.2:n.1550+164_1550+272del
ENST00000635986.2:c.1949+164_1949+272del	ENSP00000490653.2:n.1949+164_1949+272del
ENST00000636774.1:c.*516+164_*516+272del	ENSP00000489799.1:n.*516+164_*516+272del
ENST00000637238.1:c.646+204_646+312del	ENSP00000490756.1:n.646+204_646+312del
ENST00000637264.1:c.1021+164_1021+272del
ENST00000666746.1:c.1526+164_1526+272del
ENST00000670281.1:c.269+164_269+272del	ENSP00000499709.1:n.269+164_269+272del
ENST00000672071.1:n.2147+164_2147+272del
ENST00000672923.2:n.2052+164_2052+272del
ENST00000268124.9:c.1949+164_1949+272del	ENSP00000268124.5:n.1949+164_1949+272del
ENST00000442287.6:c.1949+164_1949+272del	ENSP00000399851.2:n.1949+164_1949+272del
ENST00000526314.2:c.331+164_331+272del
ENST00000526398.1:c.138+164_138+272del
ENST00000526573.1:n.35+164_35+272del
ENST00000532584.5:n.151+164_151+272del
ENST00000631044.2:c.*1332+164_*1332+272del	ENSP00000486730.1:n.*1332+164_*1332+272del
NM_001126131.1:c.1949+164_1949+272del	NP_001119603.1:n.1949+164_1949+272del
NM_002693.2:c.1949+164_1949+272del	NP_002684.1:n.1949+164_1949+272del
NM_001126131.2:c.1949+164_1949+272del	NP_001119603.1:n.1949+164_1949+272del
NM_002693.3:c.1949+164_1949+272del MANE Select	NP_002684.1:n.1949+164_1949+272del