Canonical Allele Identifier: CA2635535639

Gene: ALOX15

Linked Data

• gnomAD v4: 17-4636018-A-AT

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.4636018_4636019insT , CM000679.2:g.4636018_4636019insT	GRCh38
NC_000017.10:g.4539313_4539314insT , CM000679.1:g.4539313_4539314insT	GRCh37
NC_000017.9:g.4486062_4486063insT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000293761.8:c.952-51_952-50insA MANE Select	ENSP00000293761.3:n.952-51_952-50insA
ENST00000570836.6:c.952-51_952-50insA	ENSP00000458832.1:n.952-51_952-50insA
ENST00000293761.7:c.952-51_952-50insA	ENSP00000293761.3:n.952-51_952-50insA
ENST00000570836.5:c.952-51_952-50insA	ENSP00000458832.1:n.952-51_952-50insA
ENST00000574640.1:c.835-51_835-50insA	ENSP00000460483.1:n.835-51_835-50insA
NM_001140.3:c.952-51_952-50insA	NP_001131.3:n.952-51_952-50insA
NM_001140.4:c.952-51_952-50insA	NP_001131.3:n.952-51_952-50insA
NM_001140.5:c.952-51_952-50insA MANE Select	NP_001131.3:n.952-51_952-50insA