Canonical Allele Identifier: CA2082074019

Gene: ALOX5AP

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.30758410A= , CM000675.2:g.30758410A=	GRCh38
NC_000013.10:g.31332547A= , CM000675.1:g.31332547A=	GRCh37
NC_000013.9:g.30230547A=	NCBI36
NG_011963.2:g.49933A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380490.5:c.323+2385A= MANE Select	ENSP00000369858.3:n.323+2385A=
ENST00000380490.4:c.323+2385A=	ENSP00000369858.3:n.323+2385A=
ENST00000617770.4:c.494+2385A=	ENSP00000479870.1:n.494+2385A=
NM_001204406.1:c.494+2385A=	NP_001191335.1:n.494+2385A=
NM_001629.3:c.323+2385A=	NP_001620.2:n.323+2385A=
XM_011535025.1:c.203+2385A=	XP_011533327.1:n.203+2385A=
XM_017020522.2:c.203+2385A=	XP_016876011.1:n.203+2385A=
NM_001204406.2:c.494+2385A=	NP_001191335.1:n.494+2385A=
NM_001629.4:c.323+2385A= MANE Select	NP_001620.2:n.323+2385A=