Canonical Allele Identifier: CA287137288

Gene: ALOX15

Linked Data

• dbSNP Id: rs996444379
• gnomAD v3: 17-4636243-G-T
• gnomAD v4: 17-4636243-G-T
• MyVariant Identifiers: chr17:g.4539538G>T (hg19) ; chr17:g.4636243G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.4636243G>T , CM000679.2:g.4636243G>T	GRCh38
NC_000017.10:g.4539538G>T , CM000679.1:g.4539538G>T	GRCh37
NC_000017.9:g.4486287G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000293761.8:c.952-275C>A MANE Select	ENSP00000293761.3:n.952-275C>A
ENST00000570836.6:c.952-275C>A	ENSP00000458832.1:n.952-275C>A
ENST00000293761.7:c.952-275C>A	ENSP00000293761.3:n.952-275C>A
ENST00000570836.5:c.952-275C>A	ENSP00000458832.1:n.952-275C>A
ENST00000574640.1:c.835-275C>A	ENSP00000460483.1:n.835-275C>A
NM_001140.3:c.952-275C>A	NP_001131.3:n.952-275C>A
NM_001140.4:c.952-275C>A	NP_001131.3:n.952-275C>A
NM_001140.5:c.952-275C>A MANE Select	NP_001131.3:n.952-275C>A