Canonical Allele Identifier: CA2244455536
Gene: ALOX15 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4631484T= , CM000679.2:g.4631484T= GRCh38
NC_000017.10:g.4534779T= , CM000679.1:g.4534779T= GRCh37
NC_000017.9:g.4481528T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293761.8:c.*116A= MANE Select ENSP00000293761.3:n.*116A=
ENST00000293761.7:c.*116A= ENSP00000293761.3:n.*116A=
ENST00000570836.5:c.*116A= ENSP00000458832.1:n.*116A=
ENST00000574640.1:c.*116A= ENSP00000460483.1:n.*116A=
NM_001140.3:c.*116A= NP_001131.3:n.*116A=
NM_001140.4:c.*116A= NP_001131.3:n.*116A=
NM_001140.5:c.*116A= MANE Select NP_001131.3:n.*116A=