Canonical Allele Identifier: CA2244455398

Gene: ALOX15

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.4631199T= , CM000679.2:g.4631199T=	GRCh38
NC_000017.10:g.4534494T= , CM000679.1:g.4534494T=	GRCh37
NC_000017.9:g.4481243T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000293761.8:c.*401A= MANE Select	ENSP00000293761.3:n.*401A=
ENST00000293761.7:c.*401A=	ENSP00000293761.3:n.*401A=
ENST00000570836.5:c.*401A=	ENSP00000458832.1:n.*401A=
NM_001140.3:c.*401A=	NP_001131.3:n.*401A=
NM_001140.4:c.*401A=	NP_001131.3:n.*401A=
NM_001140.5:c.*401A= MANE Select	NP_001131.3:n.*401A=