Canonical Allele Identifier: CA2635535088

Gene: ALOX15

Linked Data

• gnomAD v4: 17-4631834-C-CCA

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.4631838_4631839dup , CM000679.2:g.4631838_4631839dup	GRCh38
NC_000017.10:g.4535133_4535134dup , CM000679.1:g.4535133_4535134dup	GRCh37
NC_000017.9:g.4481882_4481883dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000293761.8:c.1809+53_1809+54dup MANE Select	ENSP00000293761.3:n.1809+53_1809+54dup
ENST00000570836.6:c.1809+53_1809+54dup	ENSP00000458832.1:n.1809+53_1809+54dup
ENST00000293761.7:c.1809+53_1809+54dup	ENSP00000293761.3:n.1809+53_1809+54dup
ENST00000570836.5:c.1809+53_1809+54dup	ENSP00000458832.1:n.1809+53_1809+54dup
ENST00000574640.1:c.1692+53_1692+54dup	ENSP00000460483.1:n.1692+53_1692+54dup
NM_001140.3:c.1809+53_1809+54dup	NP_001131.3:n.1809+53_1809+54dup
NM_001140.4:c.1809+53_1809+54dup	NP_001131.3:n.1809+53_1809+54dup
NM_001140.5:c.1809+53_1809+54dup MANE Select	NP_001131.3:n.1809+53_1809+54dup