Canonical Allele Identifier: CA2645384359
Gene: TOE1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.45341471_45341472insTTTACCGTACATAGCACATTACAGTCAAATCCCTTCTCGTCCCAA , CM000663.2:g.45341471_45341472insTTTACCGTACATAGCACATTACAGTCAAATCCCTTCTCGTCCCAA GRCh38
NC_000001.10:g.45807143_45807144insTTTACCGTACATAGCACATTACAGTCAAATCCCTTCTCGTCCCAA , CM000663.1:g.45807143_45807144insTTTACCGTACATAGCACATTACAGTCAAATCCCTTCTCGTCCCAA GRCh37
NC_000001.9:g.45579730_45579731insTTTACCGTACATAGCACATTACAGTCAAATCCCTTCTCGTCCCAA NCBI36
NG_008189.1:g.4004_4005insACGAGAAGGGATTTGACTGTAATGTGCTATGTACGGTAAATTGGG , LRG_220:g.4004_4005insACGAGAAGGGATTTGACTGTAATGTGCTATGTACGGTAAATTGGG

Transcript Alleles

HGVS Amino-acid change
ENST00000372090.6:c.237-2_237-1insTTTACCGTACATAGCACATTACAGTCAAATCCCTTCTCGTCCCAA MANE Select ENSP00000361162.5:n.237-2_237-1insTTTACCG...
ENST00000671898.1:c.541-6956_541-6955insACGAGAAGGGATTTGACTGTAATGTGCTATGTACGGTAAATTGGG ENSP00000499896.1:n.541-6956_541-6955insA...
ENST00000372090.5:c.237-2_237-1insTTTACCGTACATAGCACATTACAGTCAAATCCCTTCTCGTCCCAA ENSP00000361162.5:n.237-2_237-1insTTTACCG...
ENST00000460057.1:n.48+128_48+129insTTTACCGTACATAGCACATTACAGTCAAATCCCTTCTCGTCCCAA
ENST00000471337.5:n.315-2_315-1insTTTACCGTACATAGCACATTACAGTCAAATCCCTTCTCGTCCCAA
ENST00000477731.5:n.456-2_456-1insTTTACCGTACATAGCACATTACAGTCAAATCCCTTCTCGTCCCAA
ENST00000495703.5:n.507-2_507-1insTTTACCGTACATAGCACATTACAGTCAAATCCCTTCTCGTCCCAA
NM_025077.3:c.237-2_237-1insTTTACCGTACATAGCACATTACAGTCAAATCCCTTCTCGTCCCAA NP_079353.3:n.237-2_237-1insTTTACCGTACATA...
XM_005270412.2:c.255-2_255-1insTTTACCGTACATAGCACATTACAGTCAAATCCCTTCTCGTCCCAA XP_005270469.1:n.255-2_255-1insTTTACCGTAC...
XM_005270413.3:c.99-2_99-1insTTTACCGTACATAGCACATTACAGTCAAATCCCTTCTCGTCCCAA XP_005270470.1:n.99-2_99-1insTTTACCGTACAT...
XM_011540569.1:c.-49+128_-49+129insTTTACCGTACATAGCACATTACAGTCAAATCCCTTCTCGTCCCAA XP_011538871.1:n.-49+128_-49+129insTTTACC...
XR_246230.2:n.514-2_514-1insTTTACCGTACATAGCACATTACAGTCAAATCCCTTCTCGTCCCAA
XR_426587.2:n.334-2_334-1insTTTACCGTACATAGCACATTACAGTCAAATCCCTTCTCGTCCCAA
XR_946532.1:n.334-2_334-1insTTTACCGTACATAGCACATTACAGTCAAATCCCTTCTCGTCCCAA
XM_005270412.4:c.255-2_255-1insTTTACCGTACATAGCACATTACAGTCAAATCCCTTCTCGTCCCAA XP_005270469.1:n.255-2_255-1insTTTACCGTAC...
XM_005270413.5:c.99-2_99-1insTTTACCGTACATAGCACATTACAGTCAAATCCCTTCTCGTCCCAA XP_005270470.1:n.99-2_99-1insTTTACCGTACAT...
XM_011540569.3:c.-49+128_-49+129insTTTACCGTACATAGCACATTACAGTCAAATCCCTTCTCGTCCCAA XP_011538871.1:n.-49+128_-49+129insTTTACC...
XM_024452837.1:c.186-2_186-1insTTTACCGTACATAGCACATTACAGTCAAATCCCTTCTCGTCCCAA XP_024308605.1:n.186-2_186-1insTTTACCGTAC...
XR_001736951.2:n.424-2_424-1insTTTACCGTACATAGCACATTACAGTCAAATCCCTTCTCGTCCCAA
XR_002959287.1:n.826-2_826-1insTTTACCGTACATAGCACATTACAGTCAAATCCCTTCTCGTCCCAA
XR_246230.4:n.424-2_424-1insTTTACCGTACATAGCACATTACAGTCAAATCCCTTCTCGTCCCAA
XR_426587.4:n.334-2_334-1insTTTACCGTACATAGCACATTACAGTCAAATCCCTTCTCGTCCCAA
XR_946532.3:n.334-2_334-1insTTTACCGTACATAGCACATTACAGTCAAATCCCTTCTCGTCCCAA
NM_025077.4:c.237-2_237-1insTTTACCGTACATAGCACATTACAGTCAAATCCCTTCTCGTCCCAA MANE Select NP_079353.3:n.237-2_237-1insTTTACCGTACATA...