Canonical Allele Identifier: CA980966777

Gene: ALOX15

Linked Data

• dbSNP Id: rs1911087267
• gnomAD v3: 17-4636117-T-TCCTCC
• gnomAD v4: 17-4636117-T-TCCTCC

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.4636126_4636130dup , CM000679.2:g.4636126_4636130dup	GRCh38
NC_000017.10:g.4539421_4539425dup , CM000679.1:g.4539421_4539425dup	GRCh37
NC_000017.9:g.4486170_4486174dup	NCBI36

Transcript Alleles

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