Canonical Allele Identifier: CA2635535029
Gene: ALOX15 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4631528_4631539del , CM000679.2:g.4631528_4631539del GRCh38
NC_000017.10:g.4534823_4534834del , CM000679.1:g.4534823_4534834del GRCh37
NC_000017.9:g.4481572_4481583del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000293761.8:c.*63_*74del MANE Select ENSP00000293761.3:n.*63_*74del
ENST00000570836.6:c.*63_*74del ENSP00000458832.1:n.*63_*74del
ENST00000293761.7:c.*63_*74del ENSP00000293761.3:n.*63_*74del
ENST00000570836.5:c.*63_*74del ENSP00000458832.1:n.*63_*74del
ENST00000574640.1:c.*63_*74del ENSP00000460483.1:n.*63_*74del
NM_001140.3:c.*63_*74del NP_001131.3:n.*63_*74del
NM_001140.4:c.*63_*74del NP_001131.3:n.*63_*74del
NM_001140.5:c.*63_*74del MANE Select NP_001131.3:n.*63_*74del