Canonical Allele Identifier: CA2244455791
Gene: ALOX15 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4632006G= , CM000679.2:g.4632006G= GRCh38
NC_000017.10:g.4535301G= , CM000679.1:g.4535301G= GRCh37
NC_000017.9:g.4482050G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293761.8:c.1692C= MANE Select ENSP00000293761.3:p.Pro564=
ENST00000570836.6:c.1692C= ENSP00000458832.1:p.Pro564=
ENST00000293761.7:c.1692C= ENSP00000293761.3:p.Pro564=
ENST00000570836.5:c.1692C= ENSP00000458832.1:p.Pro564=
ENST00000574640.1:c.1575C= ENSP00000460483.1:p.Pro525=
NM_001140.3:c.1692C= NP_001131.3:p.Pro564=
NM_001140.4:c.1692C= NP_001131.3:p.Pro564=
NM_001140.5:c.1692C= MANE Select NP_001131.3:p.Pro564=