Canonical Allele Identifier: CA497518807

Gene: ALOX15

Linked Data

• dbSNP Id: rs1555549379
• MyVariant Identifiers: chr17:g.4535160_4535162del (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.4631865_4631867del , CM000679.2:g.4631865_4631867del	GRCh38
NC_000017.10:g.4535160_4535162del , CM000679.1:g.4535160_4535162del	GRCh37
NC_000017.9:g.4481909_4481911del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000293761.8:c.1809+22_1809+24del MANE Select	ENSP00000293761.3:n.1809+22_1809+24del
ENST00000570836.6:c.1809+22_1809+24del	ENSP00000458832.1:n.1809+22_1809+24del
ENST00000293761.7:c.1809+22_1809+24del	ENSP00000293761.3:n.1809+22_1809+24del
ENST00000570836.5:c.1809+22_1809+24del	ENSP00000458832.1:n.1809+22_1809+24del
ENST00000574640.1:c.1692+22_1692+24del	ENSP00000460483.1:n.1692+22_1692+24del
NM_001140.3:c.1809+22_1809+24del	NP_001131.3:n.1809+22_1809+24del
NM_001140.4:c.1809+22_1809+24del	NP_001131.3:n.1809+22_1809+24del
NM_001140.5:c.1809+22_1809+24del MANE Select	NP_001131.3:n.1809+22_1809+24del