Canonical Allele Identifier: CA2244455551

Gene: ALOX15

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.4631499_4631517delinsATGGGAAGAGGGTGGGACT , CM000679.2:g.4631499_4631517delinsATGGGAAGAGGGTGGGACT	GRCh38
NC_000017.10:g.4534794_4534812delinsATGGGAAGAGGGTGGGACT , CM000679.1:g.4534794_4534812delinsATGGGAAGAGGGTGGGACT	GRCh37
NC_000017.9:g.4481543_4481561delinsATGGGAAGAGGGTGGGACT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000293761.8:c.*83_*101delinsAGTCCCACCCTCTTCCCAT MANE Select	ENSP00000293761.3:n.*83_*101delinsAGTCCCACCCTCTTCCCAT
ENST00000570836.6:c.*83_*101delinsAGTCCCACCCTCTTCCCAT	ENSP00000458832.1:n.*83_*101delinsAGTCCCACCCTCTTCCCAT
ENST00000293761.7:c.*83_*101delinsAGTCCCACCCTCTTCCCAT	ENSP00000293761.3:n.*83_*101delinsAGTCCCACCCTCTTCCCAT
ENST00000570836.5:c.*83_*101delinsAGTCCCACCCTCTTCCCAT	ENSP00000458832.1:n.*83_*101delinsAGTCCCACCCTCTTCCCAT
ENST00000574640.1:c.*83_*101delinsAGTCCCACCCTCTTCCCAT	ENSP00000460483.1:n.*83_*101delinsAGTCCCACCCTCTTCCCAT
NM_001140.3:c.*83_*101delinsAGTCCCACCCTCTTCCCAT	NP_001131.3:n.*83_*101delinsAGTCCCACCCTCTTCCCAT
NM_001140.4:c.*83_*101delinsAGTCCCACCCTCTTCCCAT	NP_001131.3:n.*83_*101delinsAGTCCCACCCTCTTCCCAT
NM_001140.5:c.*83_*101delinsAGTCCCACCCTCTTCCCAT MANE Select	NP_001131.3:n.*83_*101delinsAGTCCCACCCTCTTCCCAT