Canonical Allele Identifier: CA2244455583
Gene: ALOX15 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4631568_4631571delinsTGGG , CM000679.2:g.4631568_4631571delinsTGGG GRCh38
NC_000017.10:g.4534863_4534866delinsTGGG , CM000679.1:g.4534863_4534866delinsTGGG GRCh37
NC_000017.9:g.4481612_4481615delinsTGGG NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293761.8:c.*29_*32delinsCCCA MANE Select ENSP00000293761.3:n.*29_*32delinsCCCA
ENST00000570836.6:c.*29_*32delinsCCCA ENSP00000458832.1:n.*29_*32delinsCCCA
ENST00000293761.7:c.*29_*32delinsCCCA ENSP00000293761.3:n.*29_*32delinsCCCA
ENST00000570836.5:c.*29_*32delinsCCCA ENSP00000458832.1:n.*29_*32delinsCCCA
ENST00000574640.1:c.*29_*32delinsCCCA ENSP00000460483.1:n.*29_*32delinsCCCA
NM_001140.3:c.*29_*32delinsCCCA NP_001131.3:n.*29_*32delinsCCCA
NM_001140.4:c.*29_*32delinsCCCA NP_001131.3:n.*29_*32delinsCCCA
NM_001140.5:c.*29_*32delinsCCCA MANE Select NP_001131.3:n.*29_*32delinsCCCA