Canonical Allele Identifier: CA2798689571

Gene: ALOX5AP

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.30738615C>G , CM000675.2:g.30738615C>G	GRCh38
NC_000013.10:g.31312752C>G , CM000675.1:g.31312752C>G	GRCh37
NC_000013.9:g.30210752C>G	NCBI36
NG_011963.2:g.30138C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380490.5:c.70+2940C>G MANE Select	ENSP00000369858.3:n.70+2940C>G
ENST00000380490.4:c.70+2940C>G	ENSP00000369858.3:n.70+2940C>G
ENST00000617770.4:c.241+2940C>G	ENSP00000479870.1:n.241+2940C>G
NM_001204406.1:c.241+2940C>G	NP_001191335.1:n.241+2940C>G
NM_001629.3:c.70+2940C>G	NP_001620.2:n.70+2940C>G
XM_011535024.1:c.70+2940C>G	XP_011533326.1:n.70+2940C>G
NM_001204406.2:c.241+2940C>G	NP_001191335.1:n.241+2940C>G
NM_001629.4:c.70+2940C>G MANE Select	NP_001620.2:n.70+2940C>G