Canonical Allele Identifier: CA2082076298
Gene: ALOX5AP HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.30763768A= , CM000675.2:g.30763768A= GRCh38
NC_000013.10:g.31337905A= , CM000675.1:g.31337905A= GRCh37
NC_000013.9:g.30235905A= NCBI36
NG_011963.2:g.55291A=

Transcript Alleles

HGVS Amino-acid change
ENST00000380490.5:c.324-176A= MANE Select ENSP00000369858.3:n.324-176A=
ENST00000380490.4:c.324-176A= ENSP00000369858.3:n.324-176A=
ENST00000617770.4:c.495-176A= ENSP00000479870.1:n.495-176A=
NM_001204406.1:c.495-176A= NP_001191335.1:n.495-176A=
NM_001629.3:c.324-176A= NP_001620.2:n.324-176A=
XM_011535025.1:c.204-176A= XP_011533327.1:n.204-176A=
XM_017020522.2:c.204-176A= XP_016876011.1:n.204-176A=
NM_001204406.2:c.495-176A= NP_001191335.1:n.495-176A=
NM_001629.4:c.324-176A= MANE Select NP_001620.2:n.324-176A=
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