Canonical Allele Identifier: CA2635535763

Gene: ALOX15

Linked Data

• gnomAD v4: 17-4636117-TCCTCC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.4636126_4636130del , CM000679.2:g.4636126_4636130del	GRCh38
NC_000017.10:g.4539421_4539425del , CM000679.1:g.4539421_4539425del	GRCh37
NC_000017.9:g.4486170_4486174del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000293761.8:c.952-154_952-150del MANE Select	ENSP00000293761.3:n.952-154_952-150del
ENST00000570836.6:c.952-154_952-150del	ENSP00000458832.1:n.952-154_952-150del
ENST00000293761.7:c.952-154_952-150del	ENSP00000293761.3:n.952-154_952-150del
ENST00000570836.5:c.952-154_952-150del	ENSP00000458832.1:n.952-154_952-150del
ENST00000574640.1:c.835-154_835-150del	ENSP00000460483.1:n.835-154_835-150del
NM_001140.3:c.952-154_952-150del	NP_001131.3:n.952-154_952-150del
NM_001140.4:c.952-154_952-150del	NP_001131.3:n.952-154_952-150del
NM_001140.5:c.952-154_952-150del MANE Select	NP_001131.3:n.952-154_952-150del