Canonical Allele Identifier: CA2635535669

Gene: ALOX15

Linked Data

• gnomAD v4: 17-4636055-T-TC

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.4636056dup , CM000679.2:g.4636056dup	GRCh38
NC_000017.10:g.4539351dup , CM000679.1:g.4539351dup	GRCh37
NC_000017.9:g.4486100dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000293761.8:c.952-88dup MANE Select	ENSP00000293761.3:n.952-88dup
ENST00000570836.6:c.952-88dup	ENSP00000458832.1:n.952-88dup
ENST00000293761.7:c.952-88dup	ENSP00000293761.3:n.952-88dup
ENST00000570836.5:c.952-88dup	ENSP00000458832.1:n.952-88dup
ENST00000574640.1:c.835-88dup	ENSP00000460483.1:n.835-88dup
NM_001140.3:c.952-88dup	NP_001131.3:n.952-88dup
NM_001140.4:c.952-88dup	NP_001131.3:n.952-88dup
NM_001140.5:c.952-88dup MANE Select	NP_001131.3:n.952-88dup