Canonical Allele Identifier: CA2082041471
Gene: ALOX5AP HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.30738546T= , CM000675.2:g.30738546T= GRCh38
NC_000013.10:g.31312683T= , CM000675.1:g.31312683T= GRCh37
NC_000013.9:g.30210683T= NCBI36
NG_011963.2:g.30069T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000380490.5:c.70+2871T= MANE Select ENSP00000369858.3:n.70+2871T=
ENST00000380490.4:c.70+2871T= ENSP00000369858.3:n.70+2871T=
ENST00000617770.4:c.241+2871T= ENSP00000479870.1:n.241+2871T=
NM_001204406.1:c.241+2871T= NP_001191335.1:n.241+2871T=
NM_001629.3:c.70+2871T= NP_001620.2:n.70+2871T=
XM_011535024.1:c.70+2871T= XP_011533326.1:n.70+2871T=
NM_001204406.2:c.241+2871T= NP_001191335.1:n.241+2871T=
NM_001629.4:c.70+2871T= MANE Select NP_001620.2:n.70+2871T=
Search 100 bp 5'
Search 100 bp 3'