Canonical Allele Identifier: CA2244455392

Gene: ALOX15

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.4631182T= , CM000679.2:g.4631182T=	GRCh38
NC_000017.10:g.4534477T= , CM000679.1:g.4534477T=	GRCh37
NC_000017.9:g.4481226T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000293761.8:c.*418A= MANE Select	ENSP00000293761.3:n.*418A=
ENST00000293761.7:c.*418A=	ENSP00000293761.3:n.*418A=
ENST00000570836.5:c.*418A=	ENSP00000458832.1:n.*418A=
NM_001140.3:c.*418A=	NP_001131.3:n.*418A=
NM_001140.4:c.*418A=	NP_001131.3:n.*418A=
NM_001140.5:c.*418A= MANE Select	NP_001131.3:n.*418A=