Canonical Allele Identifier: CA2082041542
Gene: ALOX5AP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.30738613A= , CM000675.2:g.30738613A= GRCh38
NC_000013.10:g.31312750A= , CM000675.1:g.31312750A= GRCh37
NC_000013.9:g.30210750A= NCBI36
NG_011963.2:g.30136A=

Transcript Alleles

HGVS Amino-acid change
ENST00000380490.5:c.70+2938A= MANE Select ENSP00000369858.3:n.70+2938A=
ENST00000380490.4:c.70+2938A= ENSP00000369858.3:n.70+2938A=
ENST00000617770.4:c.241+2938A= ENSP00000479870.1:n.241+2938A=
NM_001204406.1:c.241+2938A= NP_001191335.1:n.241+2938A=
NM_001629.3:c.70+2938A= NP_001620.2:n.70+2938A=
XM_011535024.1:c.70+2938A= XP_011533326.1:n.70+2938A=
NM_001204406.2:c.241+2938A= NP_001191335.1:n.241+2938A=
NM_001629.4:c.70+2938A= MANE Select NP_001620.2:n.70+2938A=