Canonical Allele Identifier: CA2082052025

Gene: ALOX5AP

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.30745981T= , CM000675.2:g.30745981T=	GRCh38
NC_000013.10:g.31320118T= , CM000675.1:g.31320118T=	GRCh37
NC_000013.9:g.30218118T=	NCBI36
NG_011963.2:g.37504T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380490.5:c.170+1822T= MANE Select	ENSP00000369858.3:n.170+1822T=
ENST00000380490.4:c.170+1822T=	ENSP00000369858.3:n.170+1822T=
ENST00000617770.4:c.341+1822T=	ENSP00000479870.1:n.341+1822T=
NM_001204406.1:c.341+1822T=	NP_001191335.1:n.341+1822T=
NM_001629.3:c.170+1822T=	NP_001620.2:n.170+1822T=
XM_011535024.1:c.*845T=	XP_011533326.1:n.*845T=
XM_011535025.1:c.-70-644T=	XP_011533327.1:n.-70-644T=
NM_001204406.2:c.341+1822T=	NP_001191335.1:n.341+1822T=
NM_001629.4:c.170+1822T= MANE Select	NP_001620.2:n.170+1822T=