Canonical Allele Identifier: CA619513974

Gene: POLG

Linked Data

• dbSNP Id: rs1567189919
• gnomAD v2: 15-89868466-AGAGTGAGTGAGTGAGAGAGAGAGT-A
• gnomAD v3: 15-89325235-AGAGTGAGTGAGTGAGAGAGAGAGT-A
• gnomAD v4: 15-89325235-AGAGTGAGTGAGTGAGAGAGAGAGT-A
• MyVariant Identifiers: chr15:g.89868467_89868490del (hg19) ; chr15:g.89325236_89325259del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.89325259_89325282del , CM000677.2:g.89325259_89325282del	GRCh38
NC_000015.9:g.89868490_89868513del , CM000677.1:g.89868490_89868513del	GRCh37
NC_000015.8:g.87669494_87669517del	NCBI36
NG_008218.1:g.14537_14560del
NG_008218.2:g.14537_14560del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000636937.2:c.1949+191_1949+214del	ENSP00000516154.1:n.1949+191_1949+214del
ENST00000268124.11:c.1949+191_1949+214del MANE Select	ENSP00000268124.5:n.1949+191_1949+214del
ENST00000530292.3:c.1550+191_1550+214del	ENSP00000432885.2:n.1550+191_1550+214del
ENST00000635986.2:c.1949+191_1949+214del	ENSP00000490653.2:n.1949+191_1949+214del
ENST00000636774.1:c.*516+191_*516+214del	ENSP00000489799.1:n.*516+191_*516+214del
ENST00000637238.1:c.646+231_646+254del	ENSP00000490756.1:n.646+231_646+254del
ENST00000637264.1:c.1021+191_1021+214del
ENST00000666746.1:c.1526+191_1526+214del
ENST00000670281.1:c.269+191_269+214del	ENSP00000499709.1:n.269+191_269+214del
ENST00000672071.1:n.2147+191_2147+214del
ENST00000672923.2:n.2052+191_2052+214del
ENST00000268124.9:c.1949+191_1949+214del	ENSP00000268124.5:n.1949+191_1949+214del
ENST00000442287.6:c.1949+191_1949+214del	ENSP00000399851.2:n.1949+191_1949+214del
ENST00000526314.2:c.331+191_331+214del
ENST00000526398.1:c.138+191_138+214del
ENST00000526573.1:n.35+191_35+214del
ENST00000532584.5:n.151+191_151+214del
ENST00000631044.2:c.*1332+191_*1332+214del	ENSP00000486730.1:n.*1332+191_*1332+214del
NM_001126131.1:c.1949+191_1949+214del	NP_001119603.1:n.1949+191_1949+214del
NM_002693.2:c.1949+191_1949+214del	NP_002684.1:n.1949+191_1949+214del
NM_001126131.2:c.1949+191_1949+214del	NP_001119603.1:n.1949+191_1949+214del
NM_002693.3:c.1949+191_1949+214del MANE Select	NP_002684.1:n.1949+191_1949+214del