Canonical Allele Identifier: CA2244455540

Gene: ALOX15

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.4631487_4631505delinsGGAGGGTGGGACATGGGAA , CM000679.2:g.4631487_4631505delinsGGAGGGTGGGACATGGGAA	GRCh38
NC_000017.10:g.4534782_4534800delinsGGAGGGTGGGACATGGGAA , CM000679.1:g.4534782_4534800delinsGGAGGGTGGGACATGGGAA	GRCh37
NC_000017.9:g.4481531_4481549delinsGGAGGGTGGGACATGGGAA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000293761.8:c.*95_*113delinsTTCCCATGTCCCACCCTCC MANE Select	ENSP00000293761.3:n.*95_*113delinsTTCCCATGTCCCACCCTCC
ENST00000570836.6:c.*95_*113delinsTTCCCATGTCCCACCCTCC	ENSP00000458832.1:n.*95_*113delinsTTCCCATGTCCCACCCTCC
ENST00000293761.7:c.*95_*113delinsTTCCCATGTCCCACCCTCC	ENSP00000293761.3:n.*95_*113delinsTTCCCATGTCCCACCCTCC
ENST00000570836.5:c.*95_*113delinsTTCCCATGTCCCACCCTCC	ENSP00000458832.1:n.*95_*113delinsTTCCCATGTCCCACCCTCC
ENST00000574640.1:c.*95_*113delinsTTCCCATGTCCCACCCTCC	ENSP00000460483.1:n.*95_*113delinsTTCCCATGTCCCACCCTCC
NM_001140.3:c.*95_*113delinsTTCCCATGTCCCACCCTCC	NP_001131.3:n.*95_*113delinsTTCCCATGTCCCACCCTCC
NM_001140.4:c.*95_*113delinsTTCCCATGTCCCACCCTCC	NP_001131.3:n.*95_*113delinsTTCCCATGTCCCACCCTCC
NM_001140.5:c.*95_*113delinsTTCCCATGTCCCACCCTCC MANE Select	NP_001131.3:n.*95_*113delinsTTCCCATGTCCCACCCTCC