Canonical Allele Identifier: CA287132892
Gene: ALOX15 HGNC NCBI

Linked Data

dbSNP Id: rs752811780

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4631463_4631464del , CM000679.2:g.4631463_4631464del GRCh38
NC_000017.10:g.4534758_4534759del , CM000679.1:g.4534758_4534759del GRCh37
NC_000017.9:g.4481507_4481508del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000293761.8:c.*139_*140del MANE Select ENSP00000293761.3:n.*139_*140del
ENST00000293761.7:c.*139_*140del ENSP00000293761.3:n.*139_*140del
ENST00000570836.5:c.*139_*140del ENSP00000458832.1:n.*139_*140del
ENST00000574640.1:c.*139_*140del ENSP00000460483.1:n.*139_*140del
NM_001140.3:c.*139_*140del NP_001131.3:n.*139_*140del
NM_001140.4:c.*139_*140del NP_001131.3:n.*139_*140del
NM_001140.5:c.*139_*140del MANE Select NP_001131.3:n.*139_*140del