Canonical Allele Identifier: CA624854369

Gene: ALOX15

Linked Data

• dbSNP Id: rs1226097415
• gnomAD v2: 17-4534932-AG-A
• gnomAD v3: 17-4631637-AG-A
• gnomAD v4: 17-4631637-AG-A
• MyVariant Identifiers: chr17:g.4534933del (hg19) ; chr17:g.4631638del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.4631639del , CM000679.2:g.4631639del	GRCh38
NC_000017.10:g.4534934del , CM000679.1:g.4534934del	GRCh37
NC_000017.9:g.4481683del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000293761.8:c.1951del MANE Select	ENSP00000293761.3:p.Leu651CysfsTer30
ENST00000570836.6:c.1951del	ENSP00000458832.1:p.Leu651CysfsTer30
ENST00000293761.7:c.1951del	ENSP00000293761.3:p.Leu651CysfsTer30
ENST00000570836.5:c.1951del	ENSP00000458832.1:p.Leu651CysfsTer30
ENST00000574640.1:c.1834del	ENSP00000460483.1:p.Leu612CysfsTer30
NM_001140.3:c.1951del	NP_001131.3:p.Leu651CysfsTer30
NM_001140.4:c.1951del	NP_001131.3:p.Leu651CysfsTer30
NM_001140.5:c.1951del MANE Select	NP_001131.3:p.Leu651CysfsTer30