Canonical Allele Identifier: CA2082076293

Gene: ALOX5AP

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.30763758T= , CM000675.2:g.30763758T=	GRCh38
NC_000013.10:g.31337895T= , CM000675.1:g.31337895T=	GRCh37
NC_000013.9:g.30235895T=	NCBI36
NG_011963.2:g.55281T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380490.5:c.324-186T= MANE Select	ENSP00000369858.3:n.324-186T=
ENST00000380490.4:c.324-186T=	ENSP00000369858.3:n.324-186T=
ENST00000617770.4:c.495-186T=	ENSP00000479870.1:n.495-186T=
NM_001204406.1:c.495-186T=	NP_001191335.1:n.495-186T=
NM_001629.3:c.324-186T=	NP_001620.2:n.324-186T=
XM_011535025.1:c.204-186T=	XP_011533327.1:n.204-186T=
XM_017020522.2:c.204-186T=	XP_016876011.1:n.204-186T=
NM_001204406.2:c.495-186T=	NP_001191335.1:n.495-186T=
NM_001629.4:c.324-186T= MANE Select	NP_001620.2:n.324-186T=