Canonical Allele Identifier: CA397246928

Gene: ALOX15

Linked Data

• dbSNP Id: rs1381883057
• gnomAD v2: 17-4535246-A-T
• gnomAD v4: 17-4631951-A-T
• MyVariant Identifiers: chr17:g.4535246A>T (hg19) ; chr17:g.4631951A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.4631951A>T , CM000679.2:g.4631951A>T	GRCh38
NC_000017.10:g.4535246A>T , CM000679.1:g.4535246A>T	GRCh37
NC_000017.9:g.4481995A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000293761.8:c.1747T>A MANE Select	ENSP00000293761.3:p.Phe583Ile
ENST00000570836.6:c.1747T>A	ENSP00000458832.1:p.Phe583Ile
ENST00000293761.7:c.1747T>A	ENSP00000293761.3:p.Phe583Ile
ENST00000570836.5:c.1747T>A	ENSP00000458832.1:p.Phe583Ile
ENST00000574640.1:c.1630T>A	ENSP00000460483.1:p.Phe544Ile
NM_001140.3:c.1747T>A	NP_001131.3:p.Phe583Ile
NM_001140.4:c.1747T>A	NP_001131.3:p.Phe583Ile
NM_001140.5:c.1747T>A MANE Select	NP_001131.3:p.Phe583Ile