Canonical Allele Identifier: CA2244457915

Gene: ALOX15

Linked Data

• dbSNP Id: rs1911086223
• gnomAD v4: 17-4636094-TGCCGCTCCCTACGGCTCCC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.4636096_4636114del , CM000679.2:g.4636096_4636114del	GRCh38
NC_000017.10:g.4539391_4539409del , CM000679.1:g.4539391_4539409del	GRCh37
NC_000017.9:g.4486140_4486158del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000293761.8:c.952-145_952-127del MANE Select	ENSP00000293761.3:n.952-145_952-127del
ENST00000570836.6:c.952-145_952-127del	ENSP00000458832.1:n.952-145_952-127del
ENST00000293761.7:c.952-145_952-127del	ENSP00000293761.3:n.952-145_952-127del
ENST00000570836.5:c.952-145_952-127del	ENSP00000458832.1:n.952-145_952-127del
ENST00000574640.1:c.835-145_835-127del	ENSP00000460483.1:n.835-145_835-127del
NM_001140.3:c.952-145_952-127del	NP_001131.3:n.952-145_952-127del
NM_001140.4:c.952-145_952-127del	NP_001131.3:n.952-145_952-127del
NM_001140.5:c.952-145_952-127del MANE Select	NP_001131.3:n.952-145_952-127del