Canonical Allele Identifier: CA2244457956

Gene: ALOX15

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.4636166G= , CM000679.2:g.4636166G=	GRCh38
NC_000017.10:g.4539461G= , CM000679.1:g.4539461G=	GRCh37
NC_000017.9:g.4486210G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000293761.8:c.952-198C= MANE Select	ENSP00000293761.3:n.952-198C=
ENST00000570836.6:c.952-198C=	ENSP00000458832.1:n.952-198C=
ENST00000293761.7:c.952-198C=	ENSP00000293761.3:n.952-198C=
ENST00000570836.5:c.952-198C=	ENSP00000458832.1:n.952-198C=
ENST00000574640.1:c.835-198C=	ENSP00000460483.1:n.835-198C=
NM_001140.3:c.952-198C=	NP_001131.3:n.952-198C=
NM_001140.4:c.952-198C=	NP_001131.3:n.952-198C=
NM_001140.5:c.952-198C= MANE Select	NP_001131.3:n.952-198C=