Canonical Allele Identifier: CA2082041594

Gene: ALOX5AP

Linked Data

• dbSNP Id: rs1951739048

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.30738661_30738662dup , CM000675.2:g.30738661_30738662dup	GRCh38
NC_000013.10:g.31312798_31312799dup , CM000675.1:g.31312798_31312799dup	GRCh37
NC_000013.9:g.30210798_30210799dup	NCBI36
NG_011963.2:g.30184_30185dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380490.5:c.70+2986_70+2987dup MANE Select	ENSP00000369858.3:n.70+2986_70+2987dup
ENST00000380490.4:c.70+2986_70+2987dup	ENSP00000369858.3:n.70+2986_70+2987dup
ENST00000617770.4:c.241+2986_241+2987dup	ENSP00000479870.1:n.241+2986_241+2987dup
NM_001204406.1:c.241+2986_241+2987dup	NP_001191335.1:n.241+2986_241+2987dup
NM_001629.3:c.70+2986_70+2987dup	NP_001620.2:n.70+2986_70+2987dup
XM_011535024.1:c.70+2986_70+2987dup	XP_011533326.1:n.70+2986_70+2987dup
NM_001204406.2:c.241+2986_241+2987dup	NP_001191335.1:n.241+2986_241+2987dup
NM_001629.4:c.70+2986_70+2987dup MANE Select	NP_001620.2:n.70+2986_70+2987dup