Canonical Allele Identifier: CA624854377

Gene: ALOX15

Linked Data

• dbSNP Id: rs1221005669
• gnomAD v2: 17-4535122-TG-T
• gnomAD v4: 17-4631827-TG-T
• MyVariant Identifiers: chr17:g.4535123del (hg19) ; chr17:g.4631828del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.4631830del , CM000679.2:g.4631830del	GRCh38
NC_000017.10:g.4535125del , CM000679.1:g.4535125del	GRCh37
NC_000017.9:g.4481874del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000293761.8:c.1810-49del MANE Select	ENSP00000293761.3:n.1810-49del
ENST00000570836.6:c.1810-49del	ENSP00000458832.1:n.1810-49del
ENST00000293761.7:c.1810-49del	ENSP00000293761.3:n.1810-49del
ENST00000570836.5:c.1810-49del	ENSP00000458832.1:n.1810-49del
ENST00000574640.1:c.1693-49del	ENSP00000460483.1:n.1693-49del
NM_001140.3:c.1810-49del	NP_001131.3:n.1810-49del
NM_001140.4:c.1810-49del	NP_001131.3:n.1810-49del
NM_001140.5:c.1810-49del MANE Select	NP_001131.3:n.1810-49del