Canonical Allele Identifier: CA2082041453
Gene: ALOX5AP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.30738534_30738535delinsTA , CM000675.2:g.30738534_30738535delinsTA GRCh38
NC_000013.10:g.31312671_31312672delinsTA , CM000675.1:g.31312671_31312672delinsTA GRCh37
NC_000013.9:g.30210671_30210672delinsTA NCBI36
NG_011963.2:g.30057_30058delinsTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000380490.5:c.70+2859_70+2860delinsTA MANE Select ENSP00000369858.3:n.70+2859_70+2860delinsTA
ENST00000380490.4:c.70+2859_70+2860delinsTA ENSP00000369858.3:n.70+2859_70+2860delinsTA
ENST00000617770.4:c.241+2859_241+2860delinsTA ENSP00000479870.1:n.241+2859_241+2860delinsTA
NM_001204406.1:c.241+2859_241+2860delinsTA NP_001191335.1:n.241+2859_241+2860delinsTA
NM_001629.3:c.70+2859_70+2860delinsTA NP_001620.2:n.70+2859_70+2860delinsTA
XM_011535024.1:c.70+2859_70+2860delinsTA XP_011533326.1:n.70+2859_70+2860delinsTA
NM_001204406.2:c.241+2859_241+2860delinsTA NP_001191335.1:n.241+2859_241+2860delinsTA
NM_001629.4:c.70+2859_70+2860delinsTA MANE Select NP_001620.2:n.70+2859_70+2860delinsTA