Canonical Allele Identifier: CA2244457934
Gene: ALOX15 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4636126C= , CM000679.2:g.4636126C= GRCh38
NC_000017.10:g.4539421C= , CM000679.1:g.4539421C= GRCh37
NC_000017.9:g.4486170C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293761.8:c.952-158G= MANE Select ENSP00000293761.3:n.952-158G=
ENST00000570836.6:c.952-158G= ENSP00000458832.1:n.952-158G=
ENST00000293761.7:c.952-158G= ENSP00000293761.3:n.952-158G=
ENST00000570836.5:c.952-158G= ENSP00000458832.1:n.952-158G=
ENST00000574640.1:c.835-158G= ENSP00000460483.1:n.835-158G=
NM_001140.3:c.952-158G= NP_001131.3:n.952-158G=
NM_001140.4:c.952-158G= NP_001131.3:n.952-158G=
NM_001140.5:c.952-158G= MANE Select NP_001131.3:n.952-158G=