Canonical Allele Identifier: CA2244457884
Gene: ALOX15 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4636042T= , CM000679.2:g.4636042T= GRCh38
NC_000017.10:g.4539337T= , CM000679.1:g.4539337T= GRCh37
NC_000017.9:g.4486086T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293761.8:c.952-74A= MANE Select ENSP00000293761.3:n.952-74A=
ENST00000570836.6:c.952-74A= ENSP00000458832.1:n.952-74A=
ENST00000293761.7:c.952-74A= ENSP00000293761.3:n.952-74A=
ENST00000570836.5:c.952-74A= ENSP00000458832.1:n.952-74A=
ENST00000574640.1:c.835-74A= ENSP00000460483.1:n.835-74A=
NM_001140.3:c.952-74A= NP_001131.3:n.952-74A=
NM_001140.4:c.952-74A= NP_001131.3:n.952-74A=
NM_001140.5:c.952-74A= MANE Select NP_001131.3:n.952-74A=
Search 100 bp 5'
Search 100 bp 3'