Canonical Allele Identifier: CA2244457921

Gene: ALOX15

Linked Data

• dbSNP Id: rs1911086723
• gnomAD v4: 17-4636097-C-CGTA

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.4636098_4636099insTAG , CM000679.2:g.4636098_4636099insTAG	GRCh38
NC_000017.10:g.4539393_4539394insTAG , CM000679.1:g.4539393_4539394insTAG	GRCh37
NC_000017.9:g.4486142_4486143insTAG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000293761.8:c.952-130_952-129insTAC MANE Select	ENSP00000293761.3:n.952-130_952-129insTAC
ENST00000570836.6:c.952-130_952-129insTAC	ENSP00000458832.1:n.952-130_952-129insTAC
ENST00000293761.7:c.952-130_952-129insTAC	ENSP00000293761.3:n.952-130_952-129insTAC
ENST00000570836.5:c.952-130_952-129insTAC	ENSP00000458832.1:n.952-130_952-129insTAC
ENST00000574640.1:c.835-130_835-129insTAC	ENSP00000460483.1:n.835-130_835-129insTAC
NM_001140.3:c.952-130_952-129insTAC	NP_001131.3:n.952-130_952-129insTAC
NM_001140.4:c.952-130_952-129insTAC	NP_001131.3:n.952-130_952-129insTAC
NM_001140.5:c.952-130_952-129insTAC MANE Select	NP_001131.3:n.952-130_952-129insTAC