Canonical Allele Identifier: CA2082060250

Gene: ALOX5AP

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.30752304G= , CM000675.2:g.30752304G=	GRCh38
NC_000013.10:g.31326441G= , CM000675.1:g.31326441G=	GRCh37
NC_000013.9:g.30224441G=	NCBI36
NG_011963.2:g.43827G=

Transcript Alleles

HGVS	Amino-acid Change
NM_001629.4:c.241+182G= MANE Select	NP_001620.2:n.241+182G=
ENST00000380490.5:c.241+182G= MANE Select	ENSP00000369858.3:n.241+182G=
NM_001204406.1:c.412+182G=	NP_001191335.1:n.412+182G=
NM_001204406.2:c.412+182G=	NP_001191335.1:n.412+182G=
NM_001629.3:c.241+182G=	NP_001620.2:n.241+182G=
ENST00000380490.4:c.241+182G=	ENSP00000369858.3:n.241+182G=
ENST00000617770.4:c.412+182G=	ENSP00000479870.1:n.412+182G=
XM_011535025.1:c.121+182G=	XP_011533327.1:n.121+182G=
XM_017020522.2:c.121+182G=	XP_016876011.1:n.121+182G=